Method of treating androgen receptor (ar) -positive breast cancers with selective androgen receptor modulator (sarms)

ABSTRACT

This invention relates to the treatment of androgen receptor-positive breast cancer in a subject, for example a female subject. Accordingly, this invention provides methods of: a) treating a subject suffering from breast cancer; b) treating a subject suffering from metastatic breast cancer; c) treating a subject suffering from refractory breast cancer; d) treating a subject suffering from AR-positive breast cancer; e) treating a subject suffering from AR-positive refractory breast cancer; f) treating a subject suffering from AR-positive metastatic breast cancer; g) treating a subject suffering from AR-positive and ER-positive breast cancer; h) treating a subject suffering from triple negative breast cancer; i) treating a subject suffering from advanced breast cancer; j) treating a subject suffering from breast cancer that has failed SERM (tamoxifen, toremifene), aromatase inhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine), pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab (Avastin), and/or fulvestrant treatments; k) treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; l) prolonging survival of a subject with breast cancer, and/or m) prolonging the progression-free survival of a subject with breast cancer; comprising administering to the subject a therapeutically effective amount of a selective androgen receptor modulator (SARM) compound, comprising administering to the subject a therapeutically effective amount of a SARM compound of this invention.

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of United-States Provisional Ser.No. 61/671,366 filed Jul. 13, 2012 and the benefit of U.S. Ser. No.61/726,274 filed Nov. 14, 2012, which are incorporated in their entiretyherein by reference.

FIELD OF INVENTION

This invention relates to the treatment of androgen receptor-positivebreast cancer in a subject, for example a female subject. Accordingly,this invention provides methods of: a) treating a subject suffering frombreast cancer; b) treating a subject suffering from metastatic breastcancer; c) treating a subject suffering from refractory breast cancer;d) treating a subject suffering from AR-positive breast cancer; e)treating a subject suffering from AR-positive refractory breast cancer;f) treating a subject suffering from AR-positive metastatic breastcancer; g) treating a subject suffering from AR-positive and ER-positivebreast cancer; h) treating a subject suffering from AR-positive breastcancer with or without expression of estrogen receptor (ER),progesterone receptor (PR), and/or Human Epidermal Growth FactorReceptor 2 (HER2); i) treating a subject suffering from triple negativebreast cancer; j) treating a subject suffering from advanced breastcancer; k) treating a subject suffering from breast cancer that hasfailed selective estrogen receptor modulator (SERM) (tamoxifen,toremifene), aromatase inhibitor (AI), trastuzumab (Herceptin,ado-trastuzumab emtansine), pertuzumab (Perjeta), lapatinib, exemestane(Aromasin), bevacizumab (Avastin), and/or fulvestrant treatments; l)treating a subject suffering from ER positive breast cancer; m)treating, preventing, suppressing or inhibiting metastasis in a subjectsuffering from breast cancer; n) prolonging survival of a subject withbreast cancer; o) slowing the progression of breast cancer in a subject;and/or p) prolonging the progression-free survival of a subject withbreast cancer; comprising administering to the subject a therapeuticallyeffective amount of a selective androgen receptor modulator (SARM)compound.

BACKGROUND OF THE INVENTION

Breast cancer is a disease that kills over 45,000 women each year in theUnited States alone. Over 180,000 new cases of breast cancer arediagnosed annually, and it is estimated that one in eight women willdevelop breast cancer. These numbers indicate that breast cancer is oneof the most dangerous diseases facing women today. Cancer research hasbeen unable to determine the cause of breast cancer, and has not found asuitable method of therapy or prevention.

The standard of care currently includes screening the tumor for theexpression levels of the hormone receptors, estrogen receptor (ER) andprogesterone receptor (PR), and the human epidermal growth factorreceptor 2 (HER2) kinase. Currently, a woman diagnosed with breastcancer may be treated preliminarily with surgery, chemotherapy (optionalin some cases), and radiation before targeted therapy is initiated.Hormone receptor positive breast cancers are susceptible to hormonetherapies with selective estrogen receptor modulators or SERMs (e.g.,tamoxifen, toremifene), aromatase inhibitors (e.g., anastrozole), orselective estrogen receptor degraders or SERDs (e.g., fulvestrant).Hormone therapies such as aromatase inhibitors (AI) block production ofestrogens in the body (typically used in post-menopausal women), whereasSERMs and SERDs block the proliferative action of estrogens on thebreast cancer cells. HER2 positive breast cancers are susceptible toHER2 kinase inhibitors (e.g., trastuzumab and lapatinib) and aregenerally used in metastatic disease. Anti-angiogenic therapy(bevacizumab) is also approved in metastatic disease. Despite thesemultiple tiers of targeted treatments, patients often have or developrefractory forms of breast cancer. Examples of refractory breast cancerinclude primary tumors which are triple-negative (ER, PR, HER2), hormoneresistant (SERM-, SERD-, or AI-resistant), or kinase inhibitorresistant, or metastatic breast cancer tumors. Once the targetedtherapies fail or tumors metastasize, radiation and high dosechemotherapy are required to ablate the refractory breast cancer tumors.Current chemotherapies available for the treatment of refractory breastcancer include anthracyclines, taxanes, and epothilones, which aretoxic, dangerous, costly, and often are ineffective, especially in thetreatment of metastatic disease.

Abundant clinical evidence suggests that androgens normally inhibitbreast growth. For instance, women with androgen deficits have anincreased risk for developing breast cancer. Androgen signaling plays acrucial role in breast homeostasis, negating the proliferative effectsof estrogen signaling in the breast. However, when androgens transforminto estrogens (aromatase pathway), they increase cell proliferation andmammary carcinogenesis risk. Historically, the steroidal androgenreceptor agonists testosterone, fluoxymesterone, and calusterone wereused in advanced breast cancer. These agents suffered from side effectssuch as excessive virilization, cross-reactivity with the estrogenreceptor, and aromatization to estrogens. The use of steroidal androgensin advanced breast cancer pre-dates the screening of breast cancers forhormone and kinase receptors. Recently, it was found that the AR isexpressed in 50-90% of breast tumors, providing a mechanism to useandrogens as targeted therapy for AR-positive breast cancers.

Selective androgen receptor modulators (SARMs) are compounds whichdemonstrate AR-mediated tissue selective activity. Unlike theirsteroidal precursors, SARMs are non-aromatizable, generally demonstrateno activity at other steroidal receptors including ER and PR, and arenon-virilizing. Further, SARMs may be beneficial in refractory breastcancer patients due to their hypermyoanabolic effects that shouldimprove their tolerance of high-dose chemotherapy.

New innovative approaches are urgently needed at both the basic scienceand clinical levels to develop compounds which are useful for: a)treating a subject suffering from breast cancer; b) treating a subjectsuffering from metastatic breast cancer; c) treating a subject sufferingfrom refractory breast cancer; d) treating a subject suffering fromAR-positive breast cancer; e) treating a subject suffering fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; and/or h)treating, preventing, suppressing or inhibiting metastasis in a subjectsuffering from breast cancer.

SUMMARY OF THE INVENTION

In one embodiment, this invention relates to the treatment of androgenreceptor-positive breast cancer in a subject, for example a femalesubject. Accordingly, this invention provides methods for: a) treating asubject suffering from breast cancer; b) treating a subject sufferingfrom metastatic breast cancer; c) treating a subject suffering fromrefractory breast cancer; d) treating a subject suffering fromAR-positive breast cancer; e) treating a subject suffering fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; h) treating asubject suffering from AR-positive breast cancer with or withoutexpression of ER, PR, and/or HER2; i) treating a subject suffering fromtriple negative breast cancer; j) treating a subject suffering fromadvanced breast cancer; k) treating a subject suffering from breastcancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatments; l) treating a subjectsuffering from ER positive breast cancer; m) treating, preventing,suppressing or inhibiting metastasis in a subject suffering from breastcancer; n) prolonging survival of a subject with breast cancer; o)slowing the progression of breast cancer in a subject; and/or p)prolonging the progression-free survival of a subject with breastcancer; comprising administering to the subject a therapeuticallyeffective amount of a selective androgen receptor modulator (SARM)compound represented by a compound of formula I:

-   -   X is a bond, O, CH₂, NH, S, Se, PR, NO or NR;    -   G is O or S;    -   T is OH, OR, —NHCOCH₃, or NHCOR;    -   R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH₂F, CHF₂,        CF₃, CF₂CF₃, aryl, phenyl, halogen, alkenyl or OH;    -   R₁ is CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;    -   R₂ is H, F, Cl, Br, I, CH₃, CF₃, OH, CN, NO₂, NHCOCH₃, NHCOCF₃,        NHCOR, alkyl, arylalkyl, OR, NH₂, NHR, N(R)₂, SR;    -   R₃ is H, F, Cl, Br, I, CN, NO₂, COR, COOH, CONHR, CF₃, Sn(R)₃,        or R₃ together with the benzene ring to which it is attached        forms a fused ring system represented by the structure:

-   -   Z is NO₂, CN, COR, COOH, or CONHR;    -   Y is CF₃, F, Br, Cl, I, CN, or Sn(R)₃;    -   Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃, NHCOR,        NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃,        NHSO₂R, OR, COR, OCOR, OSO₂R, SO₂R or SR;    -   or Q together with the benzene ring to which it is attached is a        fused ring system represented by structure A, B or C:

-   -   n is an integer of 1-4; and    -   m is an integer of 1-3;        and/or its analog, derivative, isomer, metabolite,        pharmaceutically acceptable salt, pharmaceutical product,        hydrate, N-oxide, crystal, polymorph, prodrug or any combination        thereof, as described herein. In one embodiment, the subject is        a female subject. In one embodiment, the subject is a male        subject.

BRIEF DESCRIPTION OF THE DRAWINGS

The subject matter regarded as the invention is particularly pointed outand distinctly claimed in the concluding portion of the specification.The invention, however, both as to organization and method of operation,together with objects, features, and advantages thereof, may best beunderstood by reference to the following detailed description when readwith the accompanying drawings in which:

FIG. 1 illustrates that DHT and a compound of Formula IX inhibitMDA-MB-231 triple negative breast cancer cell growth. FIG. 1A showsMDA-MB-231 cell expression of AR following transfection. FIG. 1B showsthe IC₅₀ in AR positive MDA-MB-231 cells. FIGS. 1C, 1D, 1E, 1F, 1G, 1H,1I and 1J show the effects of DHT, to Formula IX, bicalutamide and the(R) enantiomer of Formula IX on cell survival percent (%). (FIGS. 1C,1E, 1G and 1I cells were treated in charcoal stripped FBS. FIGS. 1D, 1F,1H and 1J cells were treated in full serum).  MDA-MB-231 with lacZ; ∘MDA-MB-231 with AR 200 μL; ▴ MDA-MB-231 with AR 500 μL.

FIG. 2 illustrates that DHT and Formula IX inhibit HCC-38 triplenegative breast cancer cell growth. FIG. 2A shows HCC-38 cell expressionof AR following transfection. FIG. 2B shows the IC₅₀ in AR positiveHCC-38 cells. FIGS. 2C, 2D, 2E, 2F, 2G and 2H show the effects of DHT,Formula IX and Bicalutamide on percent (%) cell survival. (FIGS. 2C, 2Eand 2G cells were treated in charcoal stripped FBS. FIGS. 2D, 2F and 2Hcells were treated in full serum).  HCC-38 with lacZ; ∘ HCC-38 with AR200 μL; ▴ HCC-38 with AR 500 μL.

FIG. 3 illustrates that the effect of DHT and Formula IX on MDA-MB-231cells was reversed by bicalutamide. FIGS. 3A, 3B, 3C and 3D show theeffects of DHT or Formula IX in the presence or absence of bicalutamide,on percent (%) cell survival. (FIGS. 3A and 3C cells were treated incharcoal stripped FBS. FIGS. 3B and 3D cells were treated in fullserum).  lacZ and with 10 μM bicalutamide; ◯ lacZ; ▴ AR with 10 μMbicalutamide; Δ AR. FIG. 3E shows IC₅₀ values in AR positive cells inthe presence or absence of pretreatment with bicalutamide.

FIG. 4 illustrates that AR agonists inhibit triple negative breastcancer cell growth. FIGS. 4A, 4B, 4E, 4F, 4G, 4H, 4K, 4L, 4M, 4N, 4O and4P show effect of AR agonists on percent (%) cell survival. FIGS. 4C and4D show the effect of AR antagonist on percent (%) cell survival. FIGS.4I and 4J show the effect of AR non-binder on percent (%) cell survival.FIGS. 4A, 4C, 4E, 4G, 4I, 4M and 4O cells were treated in charcoalstripped FBS. FIGS. 4B, 4D, 4F, 4H, 4J, 4L, 4N and 4P cells were treatedin full serum. FIG. 4Q shows EC₅₀ and IC₅₀ values in AR positive cells.

FIG. 5 illustrates that growth inhibitory ligands are AR agonists inMDA-MB-231 cells.

FIG. 6 illustrates that growth inhibitory effects in MDA-MB-231 cellsare selective to AR. FIGS. 6A and 6B show the expression of ERα or ERβin MDA-MB-231 cells following transfection, respectively. FIGS. 6C, 6Dand 6E show the effects of to estradiol (E2) or ICI-182,780 (ICI) onpercent (%) cell survival. (FIG. 6C cells were treated in charcoalstripped serum. FIGS. 6D and 6E cells were treated in full serum).

FIG. 7 shows DHT alters the morphology of MDA-MB-231 cells.

FIG. 8 illustrates the effect of Formula VIII on steroid receptor transactivation (agonist mode).

FIG. 9 depicts a dose response curve of PR activity (antagonist mode)for compound of formula VIII, formula IX, R-enantiomer of formula IX andRU486. The closed circles () correspond to formula VIII data points(IC₅₀=17.05 nM); open circles (◯) correspond to formula IX (IC₅₀=162.9nM); closed triangles (▾) correspond to R-enantiomer of formula IX(IC₅₀=1689 nM); and open triangles (Δ) correspond to RU486 (IC₅₀=0.048nM).

FIG. 10 demonstrates that SARM (formula VIII) inhibits MDA-MB-231-ARtumor growth. Body weight (A) and tumor size (B) were measured for 35days in intact female nude mice having 150-200 mm³ tumors fromMDA-MB-231-AR triple negative breast cancer cells and then orallyadministered vehicle (

) or 30 mg/kg of formula VIII ().

FIG. 11 demonstrates that SARM (formula VIII) inhibits MDA-MB-231-ARtumor growth. Tumor size in mm³ (A) and % change in tumor size (B), aswell as tumor weight (C) were measured after 35 days in intact femalenude mice having 150-200 mm³ tumors from MDA-MB-231-AR triple negativebreast cancer cells and then receiving oral administration of vehicle or30 mg/kg of formula VIII.

FIG. 12 demonstrates the morphology of MDA-MB-231 breast cancer cellsstably transfected with AR (MDA-MB-231-AR cells). The results indicatethat AR agonists, DHT, formula IX, and formula VIII altered themorphology into a more anchored phenotype compared to vehicle,bicalutamide or an inactive isomer of formula IX. This may be indicativeof a less metastatic breast cancer phenotype.

FIG. 13 demonstrates binding and transactivation of the indicatedligands to HEK-293 (A) or MDA-MB-231 (B & C) cells. DHT, formula IX andformula VIII are agonists of AR in breast cancer cells. (Example 16)

FIG. 14 demonstrates anti-proliferative activity of DHT and SARMs inMDA-MB-231 breast cancer cells stably transfected with AR. MDA-MB-231cells stably transfected with AR using lentivirus were treated with theindicated ligands for 6 days and the number of cells counted usingcoulter counter. DHT and SARMs, but not the AR antagonist, bicalutamide,inhibited the proliferation of MDA-MB-231 triple negative breast cancercells stably transfected with AR.

DETAILED DESCRIPTION OF THE INVENTION

In one embodiment, this invention relates to the treatment of androgenreceptor-positive breast cancer in a subject. Accordingly, thisinvention provides methods of: a) treating a subject suffering frombreast cancer; b) treating a subject suffering from metastatic breastcancer; c) treating a subject suffering from refractory breast cancer;d) treating a subject suffering from AR-positive breast cancer; e)treating a subject suffering from AR-positive refractory breast cancer;f) treating a subject suffering from AR-positive metastatic breastcancer; g) treating a subject suffering from AR-positive and ER-positivebreast cancer; h) treating a subject suffering from AR-positive breastcancer with or without expression of ER, PR, and/or HER2; i) treating asubject suffering from triple negative breast cancer; j) treating asubject suffering from advanced breast cancer; k) treating a subjectsuffering from breast cancer that has failed SERM (tamoxifen,toremifene), aromatase inhibitor, trastuzumab (Herceptin,ado-trastuzumab emtansine), pertuzumab (Perjeta), lapatinib, exemestane(Aromasin), bevacizumab (Avastin), and/or fulvestrant treatment; l)treating a subject suffering from ER positive breast cancer; m)treating, preventing, suppressing or inhibiting metastasis in a subjectsuffering from breast cancer; n) prolonging survival of a subject withbreast cancer; o) slowing the progression of breast cancer in a subject;and/or p) prolonging the progression-free survival of a subject withbreast cancer; by administering to the subject a therapeuticallyeffective amount of a compound of this invention and/or its analog,derivative, isomer, metabolite, pharmaceutically acceptable salt,pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug orany combination thereof, as described herein. In one embodiment, to thesubject is a male. In one embodiment, the subject is a female.

In one embodiment of the present invention, a method is provided fortreating a subject suffering from breast cancer, comprising the step ofadministering to the subject a compound of this invention and/or itsanalog, derivative, isomer, metabolite, pharmaceutically acceptablesalt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph,prodrug or any combination thereof, in an amount effective to treatbreast cancer in the subject. In one embodiment, the subject is a femalesubject. In another embodiment, the subject is a male subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from metastatic breast cancer, comprisingthe step of administering to the subject a compound of this inventionand/or its analog, derivative, isomer, metabolite, pharmaceuticallyacceptable salt, pharmaceutical product, hydrate, N-oxide, crystal,polymorph, prodrug or any combination thereof, in an amount effective totreat metastatic breast cancer in the subject. In one embodiment, thesubject is a female subject. In another embodiment, the subject is amale subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from refractory breast cancer, comprisingthe step of administering to the subject a compound of this inventionand/or its analog, derivative, isomer, metabolite, pharmaceuticallyacceptable salt, pharmaceutical product, hydrate, N-oxide, crystal,polymorph, prodrug or any combination thereof, in an amount effective totreat refractory breast cancer in the subject. In one embodiment, thesubject is a female subject. In another embodiment, the subject is amale subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from AR-positive breast cancer, comprisingthe step of administering to the subject a compound of this inventionand/or its analog, derivative, isomer, metabolite, pharmaceuticallyacceptable salt, pharmaceutical product, hydrate, N-oxide, crystal,polymorph, prodrug or any combination thereof, in an amount effective totreat AR-positive breast cancer in the subject. In one embodiment, thesubject is a female subject. In another embodiment, the subject is amale subject.

In one embodiment, the AR-positive breast cancer is ER, PR and HER2positive. In another embodiment, the AR-positive breast cancer is ER, PRand HER2 to negative. In one embodiment, the AR-positive breast canceris ER positive, and PR andHER2 negative. In another embodiment, theAR-positive breast cancer is ER and PR positive, and HER2 negative. Inyet another embodiment, the AR-positive breast cancer is ER and HER2positive, and PR negative. In still another embodiment, the AR-positivebreast cancer is ER negative, and PR and HER2 positive. In a furtherembodiment, the AR-positive breast cancer is ER and PR negative, andHER2 positive. In still a further embodiment, the AR-positive breastcancer is ER and HER2 negative, and PR positive. In one embodiment, theAR-positive breast cancer is ER-negative. In another embodiment, theAR-positive breast cancer is ER-positive.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from AR-positive refractory breast cancer,comprising the step of administering to the subject a compound of thisinvention and/or its analog, derivative, isomer, metabolite,pharmaceutically acceptable salt, pharmaceutical product, hydrate,N-oxide, crystal, polymorph, prodrug or any combination thereof, in anamount effective to treat AR-positive refractory breast cancer in thesubject. In one embodiment, the subject is a female subject. In anotherembodiment, the subject is a male subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from AR-positive metastatic breast cancer,comprising the step of administering to the subject a compound of thisinvention and/or its analog, derivative, isomer, metabolite,pharmaceutically acceptable salt, pharmaceutical product, hydrate,N-oxide, crystal, polymorph, prodrug or any combination thereof, in anamount effective to treat AR-positive metastatic breast cancer in thesubject. In one embodiment, the subject is a female subject. In anotherembodiment, the subject is a male subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from AR-positive and ER-positive breastcancer, comprising the step of administering to the subject a compoundof this invention and/or its analog, derivative, isomer, metabolite,pharmaceutically acceptable salt, pharmaceutical product, hydrate,N-oxide, crystal, polymorph, prodrug or any combination thereof, in anamount effective to treat AR-positive metastatic breast cancer in thesubject. In one embodiment, the subject is a female subject. In anotherembodiment, the subject is a male subject.

In another embodiment of the present invention, a method is provided forto treating a subject suffering from ER-positive breast cancer,comprising the step of administering to the subject a compound of thisinvention and/or its analog, derivative, isomer, metabolite,pharmaceutically acceptable salt, pharmaceutical product, hydrate,N-oxide, crystal, polymorph, prodrug or any combination thereof, in anamount effective to treat ER-positive breast cancer in the subject. Inone embodiment, the subject is a female subject. In another embodiment,the subject is a male subject.

In one embodiment, the ER-positive breast cancer is AR-positive. Inanother embodiment, the ER-positive breast cancer is AR-negative.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from triple negative breast cancer,comprising the step of administering to the subject a compound of thisinvention and/or its analog, derivative, isomer, metabolite,pharmaceutically acceptable salt, pharmaceutical product, hydrate,N-oxide, crystal, polymorph, prodrug or any combination thereof, in anamount effective to treat triple negative breast cancer in the subject.In one embodiment, the subject is a female subject. In anotherembodiment, the subject is a male subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from advanced breast cancer, comprising thestep of administering to the subject a compound of this invention and/orits analog, derivative, isomer, metabolite, pharmaceutically acceptablesalt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph,prodrug or any combination thereof, in an amount effective to treatadvanced breast cancer in the subject. In one embodiment, the subject isa female subject. In another embodiment, the subject is a male subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from breast cancer that has failed (SERM)(tamoxifen, toremifene), aromatase inhibitor, trastuzumab (Herceptin,ado-trastuzumab emtansine), pertuzumab (Perjeta), lapatinib, exemestane(Aromasin), bevacizumab (Avastin), and/or fulvestrant treatments,comprising the step of administering to the subject a compound of thisinvention and/or its analog, derivative, isomer, metabolite,pharmaceutically acceptable salt, pharmaceutical product, hydrate,N-oxide, crystal, polymorph, prodrug or to any combination thereof, inan amount effective to treat breast cancer that has failed SERM(tamoxifen, toremifene), aromatase inhibitor, trastuzumab (Herceptin,ado-trastuzumab emtansine), pertuzumab (Perjeta), lapatinib, exemestane(Aromasin), bevacizumab (Avastin), and/or fulvestrant treatments in thesubject. In one embodiment, the subject is a female subject. In anotherembodiment, the subject is a male subject.

As used herein, in one embodiment the term “treating” may refer totreating, preventing, delaying the progression, preventing therecurrence or treating the recurrence. In one embodiment, the term“treating” refers to a reduction in morbidity, mortality, or acombination thereof, in association with breast cancer.

As used herein, the term “breast cancer” may refer to breast cancer;advanced breast cancer; metastatic breast cancer; AR-positive breastcancer; ER-positive breast cancer; AR-positive breast cancer with orwithout expression of ER, PR and/or HER2; AR-positive breast cancer withor without expression of ER; ER-positive breast cancer with or withoutexpression of AR; AR-positive and ER-positive breast cancer; refractorybreast cancer; AR-positive refractory breast cancer; ER-positiverefractory breast cancer; AR-positive metastatic breast cancer;ER-positive metastatic breast cancer; breast cancer that has failed SERM(tamoxifen, toremifene), aromatase inhibitor, trastuzumab (Herceptin,ado-trastuzumab emtansine), pertuzumab (Perjeta), lapatinib, exemestane(Aromasin), bevacizumab (Avastin), and/or fulvestrant treatments; ortriple negative breast cancer; or any combination thereof.

In one embodiment, the term “breast cancer” refers to a conditioncharacterized by anomalous rapid proliferation of abnormal cells in oneor both breasts of a subject. The abnormal cells often are referred toas “neoplastic cells,” which refers to, in some embodiments, transformedcells that can form a solid tumor. The term “tumor”, in someembodiments, refers to an abnormal mass or population of cells (i.e. twoor more cells) that result from excessive or abnormal cell division,whether malignant or benign, and pre-cancerous and cancerous cells.Malignant tumors are distinguished from benign growths or tumors inthat, in addition to uncontrolled cellular proliferation, they caninvade surrounding tissues and can metastasize.

In breast cancer, neoplastic cells may be identified in one or bothbreasts only and not in another tissue or organ, in one or both breastsand one or more adjacent tissues or organs (e.g. lymph node), or in abreast and one or more non-adjacent tissues or organs to which thebreast cancer cells have metastasized.

The term “metastasis”, in some embodiments, refers to a process in whichcancer cells travel from one organ or tissue to another non-adjacentorgan or tissue. Cancer cells in the breast(s) can spread to tissues andorgans of a subject, and conversely, cancer cells from other organs ortissue can invade or metastasize to a breast. Cancerous cells from thebreast(s) may invade or metastasize to any other organ or tissue of thebody. Breast cancer cells often invade lymph node cells and/ormetastasize to the liver, brain and/or bone and spread cancer in thesetissues and organs. The term “invasion”, in some embodiments, refers tothe spread of cancerous cells to adjacent surrounding tissues.

As used herein, the term “advanced breast cancer” refers to cancer thathas spread to other places in the body and usually cannot be cured orcontrolled with current treatment.

As used herein, the term “AR-positive breast cancer” may refer to breastcancer wherein at least a portion of the cancer cells express at leastthe androgen receptor (AR).

As used herein, the term “ER-positive breast cancer” may refer to breastcancer wherein at last a portion of the cancer cells express at leastthe estrogen receptor (ER).

As used herein, the term “triple negative breast cancer” may refer tobreast cancer cells that do not have estrogen receptors (ER),progesterone receptors (PR), or large amounts of HER2/neu protein.“Triple negative breast cancer” may also be referred to herein as“ER-negative PR-negative HER2/neu-negative breast cancer”.

As used herein, the term “refractory” may refer to breast cancer thatdoes not respond to treatment. The breast cancer may be resistant at thebeginning of treatment or it may become resistant during treatment.“Refractory breast cancer” may also be referred to herein as “resistantcancer”.

In another embodiment of the present invention, a method is provided fortreating, preventing, suppressing or inhibiting metastasis in a subjectsuffering from breast to cancer, comprising the step of administering tothe subject a compound of this invention and/or its analog, derivative,isomer, metabolite, pharmaceutically acceptable salt, pharmaceuticalproduct, hydrate, N-oxide, crystal, polymorph, prodrug or anycombination thereof, in an amount effective to treat, prevent, suppressor inhibit metastasis in the subject. In one embodiment, the subject isa female subject. In another embodiment, the subject is a male subject.

In another embodiment of the present invention, a method is provided forprolonging the survival of a subject with breast cancer, comprising thestep of administering to the subject a compound of this invention and/orits analog, derivative, isomer, metabolite, pharmaceutically acceptablesalt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph,prodrug or any combination thereof, in an amount effective to prolongthe survival of a subject with breast cancer. In one embodiment, thesubject is a female subject. In another embodiment, the subject is amale subject.

In another embodiment of the present invention, a method is provided forslowing the progression of breast cancer in a subject, comprising thestep of administering to the subject a compound of this invention and/orits analog, derivative, isomer, metabolite, pharmaceutically acceptablesalt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph,prodrug or any combination thereof, in an amount effective to slow theprogression of breast cancer in the subject. In one embodiment, thesubject is a female subject. In another embodiment, the subject is amale subject.

In another embodiment of the present invention, a method is provided forprolonging the progression-free survival of a subject with breastcancer, comprising the step of administering to the subject a compoundof this invention and/or its analog, derivative, isomer, metabolite,pharmaceutically acceptable salt, pharmaceutical product, hydrate,N-oxide, crystal, polymorph, prodrug or any combination thereof, in anamount effective to prolong the progression-free survival of a subjectwith breast cancer. In one embodiment, the subject is a female subject.In another embodiment, the subject is a male subject.

In another embodiment of the present invention, a method is provided forto lowering biomarker levels in a subject with breast cancer comprisingthe step of administering to the subject a compound of this inventionand/or its analog, derivative, isomer, metabolite, pharmaceuticallyacceptable salt, pharmaceutical product, hydrate, N-oxide, crystal,polymorph, prodrug or any combination thereof, in an amount effective tolower the biomarker level in said subject. In another embodiment, themethod comprises administering a compound of formulae I-XIV of thisinvention.

As used herein, the term “biomarker” may refer to a substance used as anindicator of a process, event, or condition. A biomarker can be abiomolecule such as a nucleic acid molecule (e.g. microRNA, genomic DNA,etc.), a protein, a polysaccharide, and the like. Biomarkers includetumor antigens and tumor markers. In one embodiment, a biomarkerindicates the presence of cancer, e.g., breast cancer. In oneembodiment, a biomarker may be used to determine the efficacy oftreatment. In one embodiment, a biomarker may be used to determine theprogression of a condition, e.g., breast cancer.

The MUC-1 associated antigen, or CA 27.29, is a cancer antigen highlyassociated with breast cancer. As used herein, the term “CA27.29biomarker” refers to a biomarker for breast cancer. In one embodiment,CA27.29 is a biomarker for advanced breast cancer.

“PSA (prostate-specific antigen) biomarker” is used as a biomarker forprostate cancer, however PSA was also found in the blood of women withbreast cancer at higher levels compared to women without breast cancer.PSA is useful also as a biomarker for breast cancer.

“CTX biomarker” and “NTX biomarker” are the C-telopeptide andN-telopeptide of collagen type I, respectively, which are used asbiomarkers of bone turnover. NTX and CTX biomarkers may be sensitiveindicators of the presence of bone metastases in breast cancer patients.

In one embodiment, a method of this invention lowers CA27.29 biomarkeris a subject. In one embodiment, a method of this invention lowers PSAin a subject. In one embodiment, a method of this invention lowers CTXbiomarker in a subject. In one embodiment of this invention, a method ofthis invention lowers NTX biomarker in a subject. In another embodiment,a method of this invention maintains the level of CA27.29 in a subject.In another embodiment, a method of this invention maintains the level ofPSA in a subject. In another embodiment, a method of this inventionmaintains the level of CTX biomarker in a subject. In anotherembodiment, a method of this invention maintains the level of NTXbiomarker. In one embodiment, the subject has breast cancer. In oneembodiment, the subject has advanced breast cancer. In anotherembodiment, the subject has refractory breast cancer. In yet anotherembodiment, the subject has AR-positive breast cancer. In still anotherembodiment, the subject has ER-positive breast cancer.

In one embodiment, the compound of this invention is an antagonist. Inanother embodiment, the compound of this invention is an agonist. In yetanother embodiment, the compound of this invention is a partialagonist/partial antagonist. In one embodiment, a compound of thisinvention is an AR agonist. In another embodiment, a compound is an ARantagonist. In yet another embodiment, a compound is a partial ARagonist and AR antagonist. In one embodiment, a compound of thisinvention is a PR agonist. In another embodiment, a compound is a PRantagonist. In yet another embodiment, a compound is a partial PRagonist and PR antagonist.

In one embodiment, a compound of this invention is an AR agonist and aPR antagonist.

The SARM compounds of this invention may be useful, in some embodiments,for: a) treatment, prevention, delaying onset of, increasing time tofirst skeletal related event (SRE), suppression or inhibition of, or thereduction of the risk of developing a skeletal-related event (SRE), suchas pathological bone fractures, surgery of the bone, radiation of thebone, spinal cord compression, new bone metastasis, and/or bone loss ina subject; b) treatment, prevention, suppression or inhibition of, orthe reduction of the risk of developing a variety of hormone-relatedconditions in a subject, for example for increasing libido; and/or forc) improving quality of life in a subject.

Osteoporosis is a systemic skeletal disease, characterized by low bonemass and deterioration of bone tissue, with a consequent increase inbone fragility and susceptibility to fracture. In the U.S., thecondition affects more than 25 million people and causes more than 1.3million fractures each year, including 500,000 spine, 250,000 hip and240,000 wrist fractures annually. Hip fractures are the most seriousconsequence of osteoporosis, with 5-20% of patients dying within oneyear, and over 50% of survivors being incapacitated. The elderly are atgreatest risk of osteoporosis, and the problem is therefore predicted toincrease significantly with the aging of the population. Worldwidefracture incidence is forecasted to increase three-fold over the next 60years, and one study estimated that there will be 4.5 million hipfractures worldwide in 2050.

Women are at greater risk of osteoporosis than men. Women experience asharp acceleration of bone loss during the five years followingmenopause. Other factors that increase the risk include smoking, alcoholabuse, a sedentary lifestyle and low calcium intake. However,osteoporosis also occurs frequently in males. It is well establishedthat the bone mineral density of males decreases with age. Decreasedamounts of bone mineral content and density correlates with decreasedbone strength, and predisposes to fracture. The molecular mechanismsunderlying the pleiotropic effects of sex-hormones in non-reproductivetissues are only beginning to be understood, but it is clear thatphysiologic concentrations of androgens and estrogens play an importantrole in maintaining bone homeostasis throughout the life-cycle.Consequently, when androgen or estrogen deprivation occurs there is aresultant increase in the rate of bone remodeling that tilts the balanceof resorption and formation to the favor of resorption that contributesto the overall loss of bone mass. In males, the natural decline insex-hormones at maturity (direct decline in androgens as well as lowerlevels of estrogens derived from peripheral aromatization of androgens)is associated with the frailty of bones. This effect is also observed inmales who have been castrated.

In one embodiment, this invention provides for the use of a compound asherein described, or its prodrug, analog, isomer, metabolite,derivative, pharmaceutically acceptable salt, pharmaceutical product,polymorph, crystal, impurity, N-oxide, hydrate or any combinationthereof, for: a) treating a bone related disorder; b) preventing a bonerelated disorder; c) suppressing a bone related disorder; d) inhibitinga bone related disorder; e) increasing a strength of a bone of asubject; f) increasing a bone mass in a subject; g) use forosteoclastogenesis inhibition.

In one embodiment, this invention provides for the use of a compound asherein described, or its prodrug, analog, isomer, metabolite,derivative, pharmaceutically acceptable salt, pharmaceutical product,polymorph, crystal, impurity, N-oxide, hydrate or any combinationthereof, for: a) accelerating bone repair; b) treating bone disorders;c) treating bone density loss; d) treating low bone mineral density(BMD); e) treating reduced bone mass; f) treating metabolic bonedisease; g) promoting bone growth or regrowth; h) promoting bonerestoration; i) promoting bone fracture repair; j) promoting boneremodeling; k) treating bone damage following reconstructive surgeryincluding of the face, hip, or joints; l) enhancing of bone strength andfunction; m) increasing cortical bone mass; n) increasing trabecularconnectivity.

In one embodiment, the bone related disorder is a genetic disorder, orin another embodiment, is induced as a result of a treatment regimen fora given disease. For example, and in one embodiment, the compounds asherein described are useful in treating a bone-related disorder thatarises as a result of cancer metastasis to bone, or in anotherembodiment, as a result of androgen-deprivation therapy, for example,given in response to prostate carcinogenesis in the subject.

As used herein, “Estrogen-deprivation therapy” may refer to therapywhich is given in response to breast cancer in a subject. Knowntreatments include treatment with SERMs, SERDs, or aromatase inhibitors(AI). For example, and in one embodiment, the compounds as hereindescribed are useful in treating a bone-related disorder that arises asa result of cancer metastasis to bone, or in another embodiment, as aresult of estrogen-deprivation therapy, for example, given in responseto breast cancer in the subject.

In one embodiment, the bone-related disorder is a loss of bone mineraldensity (BMD). In another embodiment, the bone-related disorder isosteoporosis. In another embodiment, the bone-related disorder isosteopenia. In another embodiment, the bone-related disorder isincreased bone resorption. In another embodiment, the bone-relateddisorder is bone fracture. In another embodiment, the bone-relateddisorder is bone frailty. In another embodiment, the bone-relateddisorder is any combination of osteoporosis, osteopenia, increased boneresorption, bone fracture, bone frailty and loss of BMD. Each disorderrepresents a separate embodiment of the present invention.

“Osteoporosis” refers, in one embodiment, to a thinning of the boneswith reduction in bone mass due to depletion of calcium and boneprotein. In another embodiment, osteoporosis is a systemic skeletaldisease, characterized by low bone mass and deterioration of bonetissue, with a consequent increase in bone fragility and susceptibilityto fracture. In osteoporotic patients, bone strength is abnormal, in oneembodiment, with a resulting increase in the risk of fracture. Inanother embodiment, osteoporosis depletes both the calcium and theprotein collagen normally found in the bone, in one embodiment,resulting in either abnormal bone quality or decreased bone density. Inanother embodiment, bones that are affected by osteoporosis can fracturewith only a minor fall or injury that normally would not cause a bonefracture. The fracture can be, in one embodiment, either in the form ofcracking (as in a hip fracture) or collapsing (as in a compressionfracture of the spine). The spine, hips, and wrists are common areas ofosteoporosis-induced bone fractures, although fractures can also occurin other skeletal areas. Unchecked osteoporosis can lead, in anotherembodiment, to changes in posture, physical abnormality, and decreasedmobility.

In one embodiment, the osteoporosis results from androgen deprivation.In another embodiment, the osteoporosis follows androgen deprivation. Inanother embodiment, the osteoporosis results from estrogen-deprivationtherapy. In another embodiment, the osteoporosis followsestrogen-deprivation therapy. In another embodiment, the osteoporosis isprimary osteoporosis. In another embodiment, the osteoporosis issecondary osteoporosis. In another embodiment, the osteoporosis ispostmenopausal osteoporosis. In another embodiment, the osteoporosis isjuvenile osteoporosis. In another embodiment, the osteoporosis isidiopathic osteoporosis. In another embodiment, the osteoporosis issenile osteoporosis.

In another embodiment, the primary osteoporosis is Type I primaryosteoporosis. In another embodiment, the primary osteoporosis is Type IIprimary osteoporosis. Each type of osteoporosis represents a separateembodiment of the present invention.

According to this aspect of the invention and in one embodiment, thebone-related disorder is treated with a compound as herein described, ora combination thereof. In another embodiment, other bone-stimulatingcompounds can be provided to the subject, prior to, concurrent with orfollowing administration of a compound or compounds as herein described.In one embodiment, such a bone stimulating compound may comprise naturalor synthetic materials.

In one embodiment, the bone stimulating compound may comprise a bonemorphogenetic protein (BMP), a growth factor, such as epidermal growthfactor (EGF), a fibroblast growth factor (FGF), a transforming growthfactor (TGF, an insulin growth factor (IGF), a platelet-derived growthfactor (PDGF) hedgehog proteins such as sonic, indian and deserthedgehog, a hormone such as follicle stimulating hormone, parathyroidhormone, parathyroid hormone related peptide, activins, inhibins,follistatin, frizzled, frzb or frazzled proteins, BMP binding proteinssuch as chordin and fetuin, a cytokine such as IL-3, IL-7, GM-CSF, achemokine, such as eotaxin, a collagen, osteocalcin, osteonectin andothers, as will be appreciated by one skilled in the art.

In another embodiment, the compositions for use in treating a bonedisorder of this invention may comprise a compound or compounds asherein described, an additional bone stimulating compound, or compounds,and osteogenic cells. In one embodiment, an osteogenic cell may be astem cell or progenitor cell, which may be induced to differentiate intoan osteoblast. In another embodiment, the cell may be an osteoblast. Inanother embodiment, nucleic acids which encode bone-stimulatingcompounds may be administered to the subject, which is to be consideredas part of this invention.

In one embodiment, this invention provides for the treatment,prevention, suppression or inhibition of, or the reduction of the riskof developing a skeletal-related event (SRE), such as bone fractures,surgery of the bone, radiation of the bone, spinal cord compression, newbone metastasis, bone loss, or a combination thereof in a subject withcancer, comprising administering a compound as herein described and/orits analog, derivative, isomer, metabolite, pharmaceutically acceptablesalt, pharmaceutical product, hydrate, N-oxide, or any combinationthereof. The invention relates, inter alia, to treatment of an SRE withthe compound of this invention: (a) in a subject with prostate cancerundergoing or having undergone androgen deprivation therapy (ADT); or(b) in a subject with breast cancer undergoing or having undergoneestrogen-deprivation therapy.

In one embodiment, the skeletal-related events treated using the methodsprovided herein and/or utilizing the compositions provided herein, arefractures, which in one embodiment, are pathological fractures,non-traumatic fractures, vertebral fracture, non-vertebral fractures,morphometric fractures, or a combination thereof. In some embodiments,fractures may be simple, compound, transverse, greenstick, or comminutedfractures. In one embodiment, fractures may be to any bone in the body,which in one embodiment, is a fracture in any one or more bones of thearm, wrist, hand, finger, leg, ankle, foot, toe, hip, collar bone, or acombination thereof.

In another embodiment, the methods and/or compositions provided herein,are effective in treatment, prevention, suppression, inhibition orreduction of the risk of skeletal-related events such as pathologicfractures, spinal cord compression, hypercalcemia, bone-related pain, ortheir combination.

In another embodiment, the skeletal-related events sought to be treatedusing the methods provided herein and/or utilizing the compositionsprovided herein, comprise the necessity for bone surgery and/or boneradiation, which in some embodiments, is for the treatment of painresulting in one embodiment from bone damage, or nerve compression. Inanother embodiment, the skeletal-related events sought to be treatedusing the methods provided herein and/or utilizing the compositionsprovided herein, comprise spinal cord compression, or the necessity forchanges in antineoplastic therapy, including changes in hormonaltherapy, in a subject. In some embodiments, skeletal-related eventssought to be treated using the methods provided herein and/or utilizingthe compositions provided herein, comprise treating, suppressing,preventing, reducing the incidence of, or delaying progression orseverity of bone metastases, or bone loss. In one embodiment, bone lossmay comprise osteoporosis, osteopenia, or a combination thereof. In oneembodiment, skeletal-related events may comprise any combination of theembodiments listed herein.

In one embodiment, the methods provided herein and/or utilizing thecompositions provided herein, are effective in reducing metastases tothe bone, such as in terms of number of foci, the size of foci, or acombination thereof. According to this aspect of the invention and inone embodiment, provided herein is a method of preventing or inhibitingcancer metastasis to bone in a subject, comprising the step ofadministering to the subject a composition comprising toremifene,raloxifene, tamoxifen or an analogue, functional derivative, metaboliteor a combination thereof, or a pharmaceutically acceptable salt thereof.In one embodiment, such metabolites may comprise ospemifene, fispemifeneor their combination. In one embodiment, the cancer is prostate cancer.In one embodiment, the cancer is breast cancer.

In one embodiment, the skeletal-related events are a result of cancertherapy. In one embodiment, the skeletal-related events are a result ofhormone deprivation therapy, while in another embodiment, they are aproduct of androgen deprivation therapy (ADT), and in another embodimentthey are a product of estrogen-deprivation therapy

As used herein, the term “libido”, may refer to sexual desire, or asdefined in Example 9.

As used herein, the term “quality of life” may refer to the focuses onthe health and life of a subject suffering from a condition or disease,for example suffering from breast cancer, post treatment until the endof life. It covers the physical, psychosocial, and economic issues facedby the subject, beyond the diagnosis and treatment phases. The term“quality of life” may also be referred to herein as “survivorship”. Inone embodiment, survivorship includes issues related to the ability toget health care and follow-up treatment, late effects of treatment,second cancers, and quality of life. Family members, friends, andcaregivers are also considered part of the survivorship experience.

In one embodiment, the methods of this invention are useful to asubject, which is a human. In one embodiment, the subject is male. Inanother embodiment, the subject is female. In some embodiments, whilethe methods as described herein may be useful for treating either malesor females, females may respond more advantageously to administration ofcertain compounds, for certain methods. In other embodiments, while themethods as described herein may be useful for treating either males orfemales, males may respond more advantageously to administration ofcertain compounds, for certain methods.

Selective Androgen Receptor Modulator (SARM) Compounds

In one embodiment, the compound of this invention which is effective at:a) treating a subject suffering from breast cancer; b) treating asubject suffering from metastatic breast cancer; c) treating a subjectsuffering from refractory breast cancer; d) treating a subject sufferingfrom AR-positive breast cancer; e) treating a subject suffering to fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; h) treating asubject suffering from AR-positive breast cancer with or withoutexpression of ER, PR, and/or HER2; i) treating a subject suffering fromtriple negative breast cancer; j) treating a subject suffering fromadvanced breast cancer; k) treating a subject suffering from breastcancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatment; l) treating a subject sufferingfrom ER positive breast cancer; m) treating, preventing, suppressing orinhibiting metastasis in a subject suffering from breast cancer; n)prolonging survival of a subject with breast cancer; o) slowing theprogression of breast cancer in a subject; and/or p) prolonging theprogression-free survival of a subject with breast cancer; is a compoundrepresented by a structure of formula I, and/or its analog, derivative,isomer, metabolite, pharmaceutically acceptable salt, pharmaceuticalproduct, hydrate, N-oxide, crystal, polymorph, prodrug or anycombination thereof:

-   -   X is a bond, O, CH₂, NH, S, Se, PR, NO or NR;    -   G is O or S;    -   T is OH, OR, —NHCOCH₃, or NHCOR;    -   R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH₂F, CHF₂,        CF₃, CF₂CF₃, aryl, phenyl, halogen, alkenyl or OH;    -   R₁ is CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;    -   R₂ is H, F, Cl, Br, I, CH₃, CF₃, OH, CN, NO₂, NHCOCH₃, NHCOCF₃,        NHCOR, alkyl, arylalkyl, OR, NH₂, NHR, N(R)₂, SR;    -   R₃ is H, F, Cl, Br, I, CN, NO₂, COR, COOH, CONHR, CF₃, Sn(R)₃,        or R₃ together with the benzene ring to which it is attached        forms a fused ring system represented by the structure:

-   -   Z is NO₂, CN, COR, COOH, or CONHR;    -   Y is CF₃, F, Br, Cl, I, CN, or Sn(R)₃;    -   Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃, NHCOR,        NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃,        NHSO₂R, OR, COR, OCOR, OSO₂R, SO₂R or SR;    -   or Q together with the benzene ring to which it is attached is a        fused ring system represented by structure A, B or C:

-   -   n is an integer of 1-4; and    -   m is an integer of 1-3.

In one embodiment, G in formula I is O. In another embodiment, X informula I is O. In another embodiment, T in formula I is OH. In anotherembodiment, R₁ in formula I is CH₃. In another embodiment, Z in formulaI is NO₂. In another embodiment, Z in formula I is CN. In anotherembodiment, Y in formula I is CF₃. In another embodiment, Y in formula Iis Cl. In another embodiment, Q in formula I is CN. In anotherembodiment, Q in formula I is halogen. In another embodiment, Q informula I is F. In another embodiment, Q in formula I is Cl. In anotherembodiment, Q in formula I is NHCOCH₃. In another embodiment, Q informula I is CN and R₂ is F. In another embodiment, Q in formula I is Cland R₂ is F. In another embodiment, Q in formula I is in the paraposition. In another embodiment, Z in formula I is in the para position.In another embodiment, Y in formula I is in the meta position.

The substituents Z, Y and R₃ can be in any position of the ring carryingthese substituents (hereinafter “A ring”). In one embodiment, thesubstituent Z is in the para position of the A ring. In anotherembodiment, the substituent Y is in the meta position of the A ring. Inanother embodiment, the substituent Z is in the para position of the Aring and substituent Y is in the meta position of the A ring.

The substituents Q and R₂ can be in any position of the ring carryingthese substituents (hereinafter “B ring”). In one embodiment, thesubstituent Q is in the para position of the B ring. In anotherembodiment, the substituent R₂ is in the meta position of the B ring. Inanother embodiment, the substituent Q is CN and is in the para positionof the B ring.

As contemplated herein, when the integers m and n are greater than one,the substituents R₂ and R₃ are not limited to one particularsubstituent, and can be any combination of the substituents listedabove.

In another embodiment, the compound of this invention which is effectiveat: a) treating a subject suffering from breast cancer; b) treating asubject suffering from metastatic breast cancer; c) treating a subjectsuffering from refractory breast cancer; d) treating a subject sufferingfrom AR-positive breast cancer; e) treating a subject suffering fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; h) treating asubject suffering from AR-positive breast cancer with or withoutexpression of ER, PR, and/or HER2; i) treating a subject suffering fromtriple negative breast cancer; j) treating a subject suffering fromadvanced breast cancer; k) treating a subject suffering from breastcancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatment; l) treating a subject sufferingfrom ER positive breast cancer; m) treating, preventing, suppressing orinhibiting metastasis in a subject suffering from breast cancer; n)prolonging survival of a subject with breast cancer; o) slowing theprogression of breast cancer in a subject; and/or p) prolonging theprogression-free survival of a subject with breast cancer; is a compoundrepresented by a compound of formula II, and/or its analog, derivative,isomer, metabolite, pharmaceutically acceptable salt, pharmaceuticalproduct, hydrate, N-oxide, crystal, polymorph, prodrug or anycombination thereof:

wherein

-   -   X is a bond, O, CH₂, NH, Se, PR, or NR;    -   G is O or S;    -   T is OH, OR, —NHCOCH₃, or NHCOR;    -   Z is NO₂, CN, COR, COOH or CONHR;    -   Y is I, CF₃, Br, Cl, or Sn(R)₃;    -   Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃, NHCOR,        NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃,        NHSO₂R, OR, COR, OCOR, OSO₂R, SO₂R or SR;    -   or Q together with the benzene ring to which it is attached is a        fused ring system    -   represented by structure A, B or C:

-   -   R is a C₁-C₄ alkyl, aryl, phenyl, alkenyl, hydroxyl, a C₁-C₄        haloalkyl, halogen, or haloalkenyl; and    -   R₁ is CH₃, CF₃, CH₂CH₃, or CF₂CF₃.

In one embodiment, G in formula II is O. In another embodiment, X informula II is O. In another embodiment, T in formula II is OH. Inanother embodiment, R₁ in formula II is CH₃. In another embodiment, Z informula II is NO₂. In another embodiment, Z in formula II is CN. Inanother embodiment, Y in formula II is CF₃. In another embodiment, Y informula II is halogen. In another embodiment, Y in formula II is Cl. Inanother embodiment, Q in formula II is CN. In another embodiment, Q informula II is halogen. In another embodiment, Q in formula II is Cl. Inanother embodiment, Q in formula II is F. In another embodiment, Q informula II is NHCOCH₃. In another embodiment, Q in formula II is in thepara position. In another embodiment, Z in formula II is in the paraposition. In another embodiment, Y in formula II is in the metaposition. In another embodiment, G in formula II is O, T is OH, R₁ isCH₃, X is O, Z is CN, Y is CF₃ or halogen and Q is CN or F. In anotherembodiment, G in formula II is O, T is OH, R₁ is CH₃, X is O, Z is NO₂,Y is CF₃ and Q is NHCOCH₃, F or Cl.

The substituents Z and Y can be in any position of the ring carryingthese substituents (hereinafter “A ring”). In one embodiment, thesubstituent Z is in the para position of the A ring. In anotherembodiment, the substituent Y is in the meta position of the A ring. Inanother embodiment, the substituent Z is in the para position of the Aring and substituent Y is in the meta position of the A ring.

The substituent Q can be in any position of the ring carrying thissubstituent (hereinafter “B ring”). In one embodiment, the substituent Qis in the para position of the B ring. In another embodiment, thesubstituent Q is CN and is in the para position of the B ring.

In another embodiment, the compound of this invention which is effectiveat: a) treating a subject suffering from breast cancer; b) treating asubject suffering from metastatic breast cancer; c) treating a subjectsuffering from refractory breast cancer; d) treating a subject sufferingfrom AR-positive breast cancer; e) treating a subject suffering fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; h) treating asubject suffering from AR-positive breast cancer with or withoutexpression of ER, PR, and/or HER2; i) treating a subject suffering fromtriple negative breast cancer; j) treating a subject suffering fromadvanced breast cancer; k) treating a subject suffering from breastcancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatment; l) treating a subject sufferingfrom ER positive breast cancer; m) treating, preventing, suppressing orinhibiting metastasis in a subject suffering from breast cancer; n)prolonging survival of a subject with breast cancer; o) slowing theprogression of breast cancer in a subject; and/or p) prolonging theprogression-free survival of a subject with breast cancer; is a compoundrepresented by a structure of formula III, and/or its analog,derivative, isomer, metabolite, pharmaceutically acceptable salt,pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug orany combination thereof:

wherein

-   -   Z is NO₂, CN, COOH, COR, NHCOR or CONHR;    -   Y is CF₃, F, I, Br, Cl, CN, C(R)₃ or Sn(R)₃;    -   Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃, NHCOR,        NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃,        NHSO₂R, OR, COR, OCOR, OSO₂R, SO₂R or SR;    -   or Q together with the benzene ring to which it is attached is a        fused ring system represented by structure A, B or C:

and

-   -   R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH₂F, CHF₂,        CF₃, CF₂CF₃, aryl, phenyl, halogen, alkenyl or OH.

In one embodiment, Z in formula III is NO₂. In another embodiment, Z informula III is CN. In another embodiment, Y in formula III is CF₃. Inanother embodiment, Y in formula III is Cl. In another embodiment, Y informula III is halogen. In another embodiment, Q in formula III is CN.In another embodiment, Q in formula III is halogen. In anotherembodiment, Q in formula III is F. In another embodiment, Q in formulaIII is Cl. In another embodiment, Q in formula III is NHCOCH₃. Inanother embodiment, Z is CN, Y is CF₃ or halogen, and Q is CN or F. Inanother embodiment, Z is NO₂, Y is CF₃, and Q is NHCOCH₃, F or Cl.

In another embodiment, the compound of this invention which is effectiveat: a) treating a subject suffering from breast cancer; b) treating asubject suffering from metastatic breast cancer; c) treating a subjectsuffering from refractory breast cancer; d) treating a subject sufferingfrom AR-positive breast cancer; e) treating a subject suffering fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; h) treating asubject suffering from AR-positive breast cancer with or withoutexpression of ER, PR, and/or HER2; i) treating a subject suffering fromtriple negative breast cancer; j) treating a subject suffering fromadvanced breast cancer; k) treating a subject suffering from breastcancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatment; l) treating a subject sufferingfrom ER positive breast cancer; m) treating, preventing, suppressing orinhibiting metastasis in a subject suffering from breast cancer; n)prolonging survival of a subject with breast cancer; o) slowing theprogression of breast cancer in a subject; and/or p) prolonging theprogression-free survival of a subject with breast cancer; is a compoundrepresented by a structure of formula IV, and/or its analog, derivative,isomer, metabolite, pharmaceutically acceptable salt, pharmaceuticalproduct, hydrate, N-oxide, crystal, polymorph, prodrug or anycombination thereof:

wherein

-   -   X is a bond, O, CH₂, NH, S, Se, PR, NO or NR;    -   G is O or S;    -   R₁ is CH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃;    -   T is OH, OR, —NHCOCH₃, or NHCOR;    -   R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH₂F, CHF₂,        CF₃, CF₂CF₃, aryl, phenyl, halogen, alkenyl or OH;    -   A is a ring selected from:

-   -   B is a ring selected from:

wherein

-   -   A and B cannot simultaneously be a benzene ring;    -   Z is NO₂, CN, COOH, COR, NHCOR or CONHR;    -   Y is CF₃, F, I, Br, Cl, CN, C(R)₃ or Sn(R)₃;    -   Q₁ and Q₂ are independently hydrogen, alkyl, halogen, CF₃, CN,        C(R)₃, Sn(R)₃, N(R)₂, NHCOCH₃, NHCOCF₃, NHCOR, NHCONHR, NHCOOR,        OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃, NHSO₂R, OR, COR,        OCOR, OSO₂R, SO₂R, SR,

-   -   -   Q₃ and Q₄ are independently of each other a hydrogen, alkyl,            halogen, CF₃, CN, C(R)₃, Sn(R)₃, N(R)₂, NHCOCH₃, NHCOCF₃,            NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃,            NHCSRNHSO₂CH₃, NHSO₂R, OR, COR, OCOR, OSO₂R, SO₂R or SR;        -   W₁ is O, NH, NR, NO or S; and        -   W₂ is N or NO.

In one embodiment, G in formula IV is O. In another embodiment, X informula IV is O. In another embodiment, T in formula IV is OH. Inanother embodiment, R₁ in formula IV is CH₃. In another embodiment, Z informula IV is NO₂. In another embodiment, Z in formula IV is CN. Inanother embodiment, Y in formula IV is CF₃. In another embodiment, Y informula IV is halogen. In another embodiment, Y in formula IV is Cl. Inanother embodiment, Q₁ in formula II is CN. In another embodiment, Q₁ informula IV is F. In another embodiment, Q₁ in formula IV is Cl. Inanother embodiment, Q₁ in formula II is NHCOCH₃. In another embodiment,Q₁ in Formula IV is in the para position. In another embodiment, Z informula IV is in the para position. In another embodiment, Y in formulaIV is in the meta position. In another embodiment, G in formula IV is O,T is OH, R₁ is CH₃, X is O, Z is NO₂ or CN, Y is CF₃ or halogen and Q₁is CN, F, Cl, or NHCOCH₃.

The substituents Z and Y can be in any position of the ring carryingthese substituents (hereinafter “A ring”). In one embodiment, thesubstituent Z is in the para position of the A ring. In anotherembodiment, the substituent Y is in the meta position of the A ring. Inanother embodiment, the substituent Z is in the para position of the Aring and substituent Y is in the meta position of the A ring.

The substituents Q₁ and Q₂ can be in any position of the ring carryingthese substituents (hereinafter “B ring”). In one embodiment, thesubstituent Q₁ is in the para position of the B ring. In anotherembodiment, the substituent is Q₂ is H. In another embodiment, thesubstituent Q₁ is in the para position of the B ring and the substituentis Q₂ is H. In another embodiment, the substituent Q₁ is CN and is inthe para position of the B ring, and the substituent is Q₂ is H.

As contemplated herein, other specific embodiments of compounds includedwithin the scope of the present invention, and which are useful in: a)treating a subject suffering from breast cancer; b) treating a subjectsuffering from metastatic breast cancer; c) treating a subject sufferingfrom refractory breast cancer; d) treating a subject suffering fromAR-positive breast cancer; e) treating a subject suffering fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; h) treating asubject suffering from AR-positive breast cancer with or withoutexpression of ER, PR, and/or HER2; i) treating a subject suffering fromtriple negative breast cancer; j) treating a subject suffering fromadvanced breast cancer; k) treating a subject suffering from breastcancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatment; l) treating a subject sufferingfrom ER positive breast cancer; m) treating, preventing, suppressing orinhibiting metastasis in a subject suffering from breast cancer; n)prolonging survival of a subject with breast cancer; o) slowing theprogression of breast cancer in a subject; and/or p) prolonging theprogression-free survival of a subject with breast cancer; are formulasV or VI. It is understood that included within the scope of the presentinvention are analogs, derivatives, metabolites, isomers,pharmaceutically acceptable salts, pharmaceutical products, hydrates,N-oxides, polymorphs, crystals, prodrugs or combinations thereof ofthese compounds:

-   -   wherein Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃, NHCOR,        NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃,        NHSO₂R, OR, COR, OCOR, OSO₂R, SO₂R or SR;    -   or Q together with the benzene ring to which it is attached is a        fused ring system represented by structure A, B or C:

and

-   -   R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH₂F, CHF₂,        CF₃, CF₂CF₃, aryl, phenyl, halogen, alkenyl or OH.

In one embodiment, Q in formula V or VI is CN. In one embodiment, Q inFormula V or VI is halogen. In one embodiment, Q in formula V or VI isF. In one embodiment, Q in formula V or VI is Cl. In one embodiment, Qin formula V or VI is NHCOCH₃.

In another embodiment, the compound of this invention which is effectiveat: a) treating a subject suffering from breast cancer; b) treating asubject suffering from metastatic breast cancer; c) treating a subjectsuffering from refractory breast cancer; d) treating a subject sufferingfrom AR-positive breast cancer; e) treating a subject suffering fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; h) treating asubject suffering from AR-positive breast cancer with or withoutexpression of ER, PR, and/or HER2; i) treating a subject suffering fromtriple negative breast cancer; j) treating a subject suffering fromadvanced breast cancer; k) treating a subject suffering from breastcancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatment; l) treating a subject sufferingfrom ER positive breast cancer; m) treating, preventing, suppressing orinhibiting metastasis in a subject suffering from breast cancer; n)prolonging survival of a subject with breast cancer; o) slowing theprogression of breast cancer in a subject; and/or p) prolonging theprogression-free survival of a subject with breast cancer; is a compoundrepresented by a structure of formula VII, and/or its analog,derivative, isomer, metabolite, pharmaceutically acceptable salt,pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug orany combination thereof:

wherein Z is C₁ or CF₃.

In another embodiment, the compound which is effective at: a) treating asubject suffering from breast cancer; b) treating a subject sufferingfrom metastatic breast cancer; c) treating a subject suffering fromrefractory breast cancer; d) treating a subject suffering fromAR-positive breast cancer; e) treating a subject suffering fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; h) treating asubject suffering from AR-positive breast cancer with or withoutexpression of ER, PR, and/or HER2; i) treating a subject suffering fromtriple negative breast cancer; j) treating a subject suffering fromadvanced breast cancer; k) treating a subject suffering from breastcancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatment; l) treating a subject sufferingfrom ER positive breast cancer; m) treating, preventing, suppressing orinhibiting metastasis in a subject suffering from breast cancer; n)prolonging survival of a subject with breast cancer; o) slowing theprogression of breast cancer in a subject; and/or p) prolonging theprogression-free survival of a subject with breast cancer; is a compoundrepresented by a structure of formula VIII, and/or its analog,derivative, isomer, metabolite, pharmaceutically acceptable salt,pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug orany combination thereof:

In another embodiment, the compound which is effective at: a) treating asubject suffering from breast cancer; b) treating a subject sufferingfrom metastatic breast cancer; c) treating a subject suffering fromrefractory breast cancer; d) treating a subject suffering fromAR-positive breast cancer; e) treating a subject suffering fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; h) treating asubject suffering from AR-positive breast cancer with or withoutexpression of ER, PR, and/or HER2; i) treating a subject suffering fromtriple negative breast cancer; j) to treating a subject suffering fromadvanced breast cancer; k) treating a subject suffering from breastcancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatment; l) treating a subject sufferingfrom ER positive breast cancer; m) treating, preventing, suppressing orinhibiting metastasis in a subject suffering from breast cancer; n)prolonging survival of a subject with breast cancer; o) slowing theprogression of breast cancer in a subject; and/or p) prolonging theprogression-free survival of a subject with breast cancer; is a compoundrepresented by a structure of formula IX, and/or its analog, derivative,isomer, metabolite, pharmaceutically acceptable salt, pharmaceuticalproduct, hydrate, N-oxide, crystal, polymorph, prodrug or anycombination thereof:

In another embodiment, the compound which is effective at: a) treating asubject suffering from breast cancer; b) treating a subject sufferingfrom metastatic breast cancer; c) treating a subject suffering fromrefractory breast cancer; d) treating a subject suffering fromAR-positive breast cancer; e) treating a subject suffering fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; h) treating asubject suffering from AR-positive breast cancer with or withoutexpression of ER, PR, and/or HER2; i) treating a subject suffering fromtriple negative breast cancer; j) treating a subject suffering fromadvanced breast cancer; k) treating a subject suffering from breastcancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatment; l) treating a subject sufferingfrom ER positive breast cancer; m) treating, preventing, suppressing orinhibiting metastasis in a subject suffering from breast cancer; n)prolonging survival of a subject with breast cancer; o) slowing theprogression of breast cancer in a subject; and/or p) prolonging theprogression-free survival of a subject with breast cancer; is a compoundrepresented by a structure of formula X, and/or its analog, derivative,isomer, metabolite, pharmaceutically acceptable salt, pharmaceuticalproduct, hydrate, N-oxide, crystal, polymorph, prodrug or anycombination thereof:

In another embodiment, the compound which is effective at: a) treating asubject suffering from breast cancer; b) treating a subject sufferingfrom metastatic breast cancer; c) treating a subject suffering fromrefractory breast cancer; d) treating a subject suffering fromAR-positive breast cancer; e) treating a subject suffering fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; h) treating asubject suffering from AR-positive breast cancer with or withoutexpression of ER, PR, and/or HER2; i) treating a subject suffering fromtriple negative breast cancer; j) treating a subject suffering fromadvanced breast cancer; k) treating a subject suffering from breastcancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatment; l) treating a subject sufferingfrom ER positive breast cancer; m) treating, preventing, suppressing orinhibiting metastasis in a subject suffering from breast cancer; n)prolonging survival of a subject with breast cancer; o) slowing theprogression of breast cancer in a subject; and/or p) prolonging theprogression-free survival of a subject with breast cancer; is a compoundrepresented by a structure of formula XI, and/or its analog, derivative,isomer, metabolite, pharmaceutically acceptable salt, pharmaceuticalproduct, hydrate, N-oxide, crystal, polymorph, prodrug or anycombination thereof:

In another embodiment, the compound which is effective at: a) treating ato subject suffering from breast cancer; b) treating a subject sufferingfrom metastatic breast cancer; c) treating a subject suffering fromrefractory breast cancer; d) treating a subject suffering fromAR-positive breast cancer; e) treating a subject suffering fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; h) treating asubject suffering from AR-positive breast cancer with or withoutexpression of ER, PR, and/or HER2; i) treating a subject suffering fromtriple negative breast cancer; j) treating a subject suffering fromadvanced breast cancer; k) treating a subject suffering from breastcancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatment; l) treating a subject sufferingfrom ER positive breast cancer; m) treating, preventing, suppressing orinhibiting metastasis in a subject suffering from breast cancer; n)prolonging survival of a subject with breast cancer; o) slowing theprogression of breast cancer in a subject; and/or p) prolonging theprogression-free survival of a subject with breast cancer; is a compoundrepresented by a structure of formula XII, and/or its analog,derivative, isomer, metabolite, pharmaceutically acceptable salt,pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug orany combination thereof:

In another embodiment, the compound which is effective at: a) treating asubject suffering from breast cancer; b) treating a subject sufferingfrom metastatic breast cancer; c) treating a subject suffering fromrefractory breast cancer; d) treating a subject suffering fromAR-positive breast cancer; e) treating a subject suffering fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; h) treating asubject suffering from AR-positive breast cancer with or withoutexpression of to ER, PR, and/or HER2; i) treating a subject sufferingfrom triple negative breast cancer; j) treating a subject suffering fromadvanced breast cancer; k) treating a subject suffering from breastcancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatment; l) treating a subject sufferingfrom ER positive breast cancer; m) treating, preventing, suppressing orinhibiting metastasis in a subject suffering from breast cancer; n)prolonging survival of a subject with breast cancer; o) slowing theprogression of breast cancer in a subject; and/or p) prolonging theprogression-free survival of a subject with breast cancer; is a compoundrepresented by a compound of formula XIII, and/or its analog,derivative, isomer, metabolite, pharmaceutically acceptable salt,pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug orany combination thereof:

In another embodiment, the compound which is effective at: a) treating asubject suffering from breast cancer; b) treating a subject sufferingfrom metastatic breast cancer; c) treating a subject suffering fromrefractory breast cancer; d) treating a subject suffering fromAR-positive breast cancer; e) treating a subject suffering fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; h) treating asubject suffering from AR-positive breast cancer with or withoutexpression of ER, PR, and/or HER2; i) treating a subject suffering fromtriple negative breast cancer; j) treating a subject suffering fromadvanced breast cancer; k) treating a subject suffering from breastcancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, to trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatment; l) treating a subject sufferingfrom ER positive breast cancer; m) treating, preventing, suppressing orinhibiting metastasis in a subject suffering from breast cancer; n)prolonging survival of a subject with breast cancer; o) slowing theprogression of breast cancer in a subject; and/or p) prolonging theprogression-free survival of a subject with breast cancer; is a compoundrepresented by a structure of formula XIV, and/or its analog,derivative, isomer, metabolite, pharmaceutically acceptable salt,pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug orany combination thereof:

In one embodiment, the methods of the present invention compriseadministering an analog of the compound of formula I-XIV. In anotherembodiment, the methods of the present invention comprise administeringa derivative of the compound of formula I-XIV. In another embodiment,the methods of the present invention comprise administering an isomer ofthe compound of formula I-XIV. In another embodiment, the methods of thepresent invention comprise administering a metabolite of the compound offormula I-XIV. In another embodiment, the methods of the presentinvention comprise administering a pharmaceutically acceptable salt ofthe compound of formula I-XIV. In another embodiment, the methods of thepresent invention comprise administering a pharmaceutical product of thecompound of formula I-XIV. In another embodiment, the methods of thepresent invention comprise administering a hydrate of the compound offormula I-XIV. In another embodiment, the methods of the presentinvention comprise administering an N-oxide of the compound of formulaI-XIV. In another embodiment, the methods of the present inventioncomprise administering a polymorph of the compound of formula I-XIV. Inanother embodiment, the methods of the present invention compriseadministering a crystal of the compound of formula I-XIV. In anotherembodiment, the methods of the present invention comprise administeringa prodrug of the compound of formula I-XIV. In another embodiment, themethods of the present invention comprise administering a combination ofany of an analog, derivative, metabolite, isomer, pharmaceuticallyacceptable salt, pharmaceutical product, hydrate, N-oxide, polymorph,crystal or prodrug of the compound of formula I-XIV.

In one embodiment, the methods of this invention comprise administeringa compound of Formula I-XIV. In another embodiment, the methods of thisinvention comprise administering a compound of Formula I. In anotherembodiment, the methods of this invention comprise administering acompound of Formula II. In another embodiment, the methods of thisinvention comprise administering a compound of Formula III. In anotherembodiment, the methods of this invention comprise administering acompound of Formula IV. In another embodiment, the methods of thisinvention comprise administering a compound of Formula V. In anotherembodiment, the methods of this invention comprise administering acompound of Formula VI. In another embodiment, the methods of thisinvention comprise administering a compound of Formula VII. In anotherembodiment, the methods of this invention comprise administering acompound of Formula VIII. In another embodiment, the methods of thisinvention comprise administering a compound of Formula IX. In anotherembodiment, the methods of this invention comprise administering acompound of Formula X. In another embodiment, the methods of thisinvention comprise administering a compound of Formula XI. In anotherembodiment, the methods of this invention comprise administering acompound of Formula XII. In another embodiment, the methods of thisinvention comprise administering a compound of Formula XIII. In anotherembodiment, the methods of this invention comprise administering acompound of Formula XIV.

The compounds of the present invention, either alone or as apharmaceutical composition, are useful for: a) treating a subjectsuffering from breast cancer; b) treating a subject suffering frommetastatic breast cancer; c) treating a subject suffering fromrefractory breast cancer; d) treating a subject suffering fromAR-positive breast cancer; e) treating a subject suffering fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; h) treating asubject suffering from AR-positive breast cancer with or withoutexpression of ER, PR, and/or HER2; i) treating a subject suffering fromtriple negative breast cancer; j) treating a subject suffering fromadvanced breast cancer; k) treating a subject suffering from breastcancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatment; l) treating a subject sufferingfrom ER positive breast cancer; m) treating, preventing, suppressing orinhibiting metastasis in a subject suffering from breast cancer; n)prolonging survival of a subject with breast cancer; o) slowing theprogression of breast cancer in a subject; and/or p) prolonging theprogression-free survival of a subject with breast cancer.

The compounds of the present invention offer a significant advance oversteroidal androgen treatment since treatment of breast cancer with thesecompounds will not be accompanied by serious side effects, inconvenientmodes of administration, or high costs and still have the advantages oforal bioavailability, lack of cross-reactivity with other steroidreceptors, and long biological half-lives.

In one embodiment, this invention relates to the treatment of androgenreceptor-positive breast cancer in a subject. Accordingly, thisinvention provides methods of: a) treating a subject suffering frombreast cancer; b) treating a subject suffering from metastatic breastcancer; c) treating a subject suffering from refractory breast cancer;d) treating a subject suffering from AR-positive breast cancer; e)treating a subject suffering from AR-positive refractory breast cancer;f) treating a subject suffering from AR-positive metastatic breastcancer; g) treating a subject suffering from AR-positive and ER-positivebreast cancer; h) treating a subject suffering from AR-positive breastcancer with or without expression of ER, PR, and/or HER2; i) treating asubject suffering from triple negative breast cancer; j) treating asubject suffering from advanced breast cancer; k) treating a subjectsuffering from breast cancer that has failed SERM (tamoxifen,toremifene), aromatase inhibitor, trastuzumab (Herceptin,ado-trastuzumab emtansine), pertuzumab (Perjeta), lapatinib, exemestane(Aromasin), bevacizumab (Avastin), and/or fulvestrant treatment; l)treating a subject suffering from ER positive breast cancer; m)treating, preventing, suppressing or inhibiting metastasis in a subjectsuffering from breast cancer; n) prolonging survival of a subject withbreast cancer; o) slowing the progression of breast cancer in a subject;and/or p) prolonging the progression-free survival of a subject withbreast cancer; by administering to the subject a therapeuticallyeffective to amount of a selective androgen receptor modulator offormulas I-XIV of this invention, and/or its analog, derivative, isomer,metabolite, pharmaceutically acceptable salt, pharmaceutical product,hydrate, N-oxide, crystal, polymorph, prodrug or any combinationthereof, as described herein.

As defined herein, the term “isomer” includes, but is not limited to,optical isomers and analogs, structural isomers and analogs,conformational isomers and analogs, and the like. As used herein, theterm “isomer” may also be referred to herein as an “enantiomer” havingall of the qualities and properties of an “isomer”.

In one embodiment, this invention encompasses the use of various opticalisomers of the selective androgen receptor modulator. It will beappreciated by those skilled in the art that the selective androgenreceptor modulators of the present invention contain at least one chiralcenter. Accordingly, the selective androgen receptor modulators used inthe methods of the present invention may exist in, and be isolated in,optically-active or racemic forms. Some compounds may also exhibitpolymorphism. It is to be understood that the present inventionencompasses any racemic, optically-active, polymorphic, orstereoisomeric form, or any combination thereof, which form possessesproperties useful in the treatment of androgen-related conditionsdescribed herein. In one embodiment, the selective androgen receptormodulators are the pure (R)-isomers. In another embodiment, theselective androgen receptor modulators are the pure (S)-isomers. Inanother embodiment, the selective androgen receptor modulators are amixture of the (R) and the (S) isomers. In another embodiment, theselective androgen receptor modulators are a racemic mixture comprisingan equal amount of the (R) and the (S) isomers. It is well known in theart how to prepare optically-active forms (for example, by resolution ofthe racemic form by recrystallization techniques, by synthesis fromoptically-active starting materials, by chiral synthesis, or bychromatographic separation using a chiral stationary phase).

The invention includes “pharmaceutically acceptable salts” of thecompounds of this invention, which may be produced, by reaction of acompound of this invention with an acid or base.

The invention includes pharmaceutically acceptable salts ofamino-substituted compounds with organic and inorganic acids, forexample, citric acid and hydrochloric acid. The invention also includesN-oxides of the amino substituents of the compounds described herein.Pharmaceutically acceptable salts can also be prepared from the phenoliccompounds by treatment with inorganic bases, for example, sodiumhydroxide. Also, esters of the phenolic compounds can be made withaliphatic and aromatic carboxylic acids, for example, acetic acid andbenzoic acid esters.

Suitable pharmaceutically-acceptable salts of the compounds of FormulaI-XIV may be prepared from an inorganic acid or from an organic acid. Inone embodiment, examples of inorganic salts of the compounds of thisinvention are bisulfates, borates, bromides, chlorides, hemisulfates,hydrobromates, hydrochlorates, 2-hydroxyethylsulfonates(hydroxyethanesulfonates), iodates, iodides, isothionates, nitrates,persulfates, phosphate, sulfates, sulfamates, sulfanilates, sulfonicacids (alkylsulfonates, arylsulfonates, halogen substitutedalkylsulfonates, halogen substituted arylsulfonates), sulfonates andthiocyanates.

In one embodiment, examples of organic salts of the compounds of thisinvention may be selected from aliphatic, cycloaliphatic, aromatic,araliphatic, heterocyclic, carboxylic and sulfonic classes of organicacids, examples of which are acetates, arginines, aspartates,ascorbates, adipates, anthranilates, algenates, alkane carboxylates,substituted alkane carboxylates, alginates, benzenesulfonates,benzoates, bisulfates, butyrates, bicarbonates, bitartrates, citrates,camphorates, camphorsulfonates, cyclohexylsulfamates,cyclopentanepropionates, calcium edetates, camsylates, carbonates,clavulanates, cinnamates, dicarboxylates, digluconates,dodecylsulfonates, dihydrochlorides, decanoates, enanthuates,ethanesulfonates, edetates, edisylates, estolates, esylates, fumarates,formates, fluorides, galacturonates gluconates, glutamates, glycolates,glucorate, glucoheptanoates, glycerophosphates, gluceptates,glycollylarsanilates, glutarates, glutamate, heptanoates, hexanoates,hydroxymaleates, hydroxycarboxlic acids, hexylresorcinates,hydroxybenzoates, hydroxynaphthoate, hydrofluorate, lactates,lactobionates, laurates, malates, maleates,methylenebis(beta-oxynaphthoate), malonates, mandelates, mesylates,methane sulfonates, methylbromides, methylnitrates, methylsulfonates,monopotassium maleates, mucates, monocarboxylates, mitrates,naphthalenesulfonates, 2-naphthalenesulfonates, nicotinates, napsylates,N-methylglucamines, oxalates, octanoates, oleates, pamoates,phenylacetates, picrates, phenylbenzoates, pivalates, propionates,phthalates, phenylacetate, pectinates, phenylpropionates, palmitates,pantothenates, polygalacturates, pyruvates, quinates, salicylates,succinates, stearates, sulfanilate, subacetates, tartrates,theophyllineacetates, p-toluenesulfonates (tosylates),trifluoroacetates, terephthalates, tannates, teoclates, trihaloacetates,triethiodide, tricarboxylates, undecanoates and valerates.

In one embodiment, the salts may be formed by conventional means, suchas by reacting the free base or free acid form of the product with oneor more equivalents of the appropriate acid or base in a solvent ormedium in which the salt is insoluble or in a solvent such as water,which is removed in vacuo or by freeze drying or by exchanging the ionsof a existing salt for another ion or suitable ion-exchange resin.

This invention further includes derivatives of the selective androgenreceptor modulators. The term “derivatives” includes but is not limitedto ether derivatives, acid derivatives, amide derivatives, esterderivatives and the like. In addition, this invention further includeshydrates of the selective androgen receptor modulators. The term“hydrate” includes but is not limited to hemihydrate, monohydrate,dihydrate, trihydrate and the like.

This invention further includes metabolites of the selective androgenreceptor modulators. The term “metabolite” means any substance producedfrom another substance by metabolism or a metabolic process.

This invention further includes pharmaceutical products of the selectiveandrogen receptor modulators. The term “pharmaceutical product” means acomposition suitable for pharmaceutical use (pharmaceuticalcomposition), as defined herein.

This invention further includes prodrugs of the selective androgenreceptor modulators. The term “prodrug” means a substance which can beconverted in vivo into a biologically active agent by such reactions ashydrolysis, esterification, de-esterification, activation, saltformation and the like.

This invention further includes crystals of the selective androgenreceptor modulators. Furthermore, this invention provides polymorphs ofthe selective androgen receptor modulators. The term “crystal” means asubstance in a crystalline state. The term to “polymorph” refers to aparticular crystalline state of a substance, having particular physicalproperties such as X-ray diffraction, IR spectra, melting point, and thelike.

In one embodiment of the present invention, a method is provided fortreating a subject suffering from breast cancer, comprising the step ofadministering to the subject a compound of this invention and/or itsanalog, derivative, isomer, metabolite, pharmaceutically acceptablesalt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph,prodrug or any combination thereof, in an amount effective to treatbreast cancer in the subject. In one embodiment, the subject is a femalesubject. In another embodiment, the subject is a male subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from metastatic breast cancer, comprisingthe step of administering to the subject a selective androgen receptormodulator of formulas I-XIV of this invention and/or its analog,derivative, isomer, metabolite, pharmaceutically acceptable salt,pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug orany combination thereof, in an amount effective to treat metastaticbreast cancer in the subject. In one embodiment, the subject is a femalesubject. In another embodiment, the subject is a male subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from refractory breast cancer, comprisingthe step of administering to the subject a selective androgen receptormodulator of formulas I-XIV of this invention and/or its analog,derivative, isomer, metabolite, pharmaceutically acceptable salt,pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug orany combination thereof, in an amount effective to treat refractorybreast cancer in the subject. In one embodiment, the subject is a femalesubject. In another embodiment, the subject is a male subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from AR-positive breast cancer, comprisingthe step of administering to the subject a selective androgen receptormodulator of formulas I-XIV of this invention and/or its analog,derivative, isomer, metabolite, pharmaceutically to acceptable salt,pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug orany combination thereof, in an amount effective to treat AR-positivebreast cancer in the subject. In one embodiment, the subject is a femalesubject. In another embodiment, the subject is a male subject.

In one embodiment, the AR-positive breast cancer is ER, PR and HER2positive. In another embodiment, the AR-positive breast cancer is ER, PRand HER2 negative. In one embodiment, the AR-positive breast cancer isER positive, and PR and HER2 negative. In another embodiment, theAR-positive breast cancer is ER and PR positive, and HER2 negative. Inyet another embodiment, the AR-positive breast cancer is ER and HER2positive, and PR negative. In still another embodiment, the AR-positivebreast cancer is ER negative, and PR and HER2 positive. In a furtherembodiment, the AR-positive breast cancer is ER and PR negative, andHER2 positive. In still a further embodiment, the AR-positive breastcancer is ER and HER2 negative, and PR positive. In one embodiment, theAR-positive breast cancer is ER-negative. In another embodiment, theAR-positive breast cancer is ER-positive.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from AR-positive refractory breast cancer,comprising the step of administering to the subject a selective androgenreceptor modulator of formulas I-XIV of this invention and/or itsanalog, derivative, isomer, metabolite, pharmaceutically acceptablesalt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph,prodrug or any combination thereof, in an amount effective to treatAR-positive refractory breast cancer in the subject. In one embodiment,the subject is a female subject. In another embodiment, the subject is amale subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from AR-positive metastatic breast cancer,comprising the step of administering to the subject a selective androgenreceptor modulator of formulas I-XIV of this invention and/or itsanalog, derivative, isomer, metabolite, pharmaceutically acceptablesalt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph,prodrug or any combination thereof, in an amount effective to treatAR-positive metastatic breast cancer in the subject. In one embodiment,the subject is a female subject. In another embodiment, the subject is amale subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from ER-positive breast cancer, comprisingthe step of administering to the subject a selective androgen receptormodulator of formulas I-XIV of this invention and/or its analog,derivative, isomer, metabolite, pharmaceutically acceptable salt,pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug orany combination thereof, in an amount effective to treat ER-positivebreast cancer in the subject. In one embodiment, the subject is a femalesubject. In another embodiment, the subject is a male subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from AR-positive and ER-positive breastcancer, comprising the step of administering to the subject a selectiveandrogen receptor modulator of formulas I-XIV of this invention and/orits analog, derivative, isomer, metabolite, pharmaceutically acceptablesalt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph,prodrug or any combination thereof, in an amount effective to treatAR-positive metastatic breast cancer in the subject. In one embodiment,the subject is a female subject. In another embodiment, the subject is amale subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from ER-positive refractory breast cancer,comprising the step of administering to the subject a selective androgenreceptor modulator of formulas I-XIV of this invention and/or itsanalog, derivative, isomer, metabolite, pharmaceutically acceptablesalt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph,prodrug or any combination thereof, in an amount effective to treatER-positive refractory breast cancer in the subject. In one embodiment,the subject is a female subject. In another embodiment, the subject is amale subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from ER-positive metastatic breast cancer,comprising the step of administering to the subject a selective androgenreceptor modulator of formulas I-XIV of this invention and/or itsanalog, derivative, isomer, metabolite, pharmaceutically acceptablesalt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph,prodrug or any combination thereof, in an amount effective to treatER-positive metastatic breast to cancer in the subject. In oneembodiment, the subject is a female subject. In another embodiment, thesubject is a male subject.

In one embodiment, an ER-positive breast cancer is AR-positive. Inanother embodiment, an ER-positive breast cancer is AR-negative.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from advanced breast cancer, comprising thestep of administering to the subject a selective androgen receptormodulator of formulas I-XIV of this invention and/or its analog,derivative, isomer, metabolite, pharmaceutically acceptable salt,pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug orany combination thereof, in an amount effective to treat advanced breastcancer in the subject. In one embodiment, the subject is a femalesubject. In another embodiment, the subject is a male subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from AR-positive and ER-positive breastcancer, comprising the step of administering to the subject a selectiveandrogen receptor modulator of formulas I-XIV of this invention and/orits analog, derivative, isomer, metabolite, pharmaceutically acceptablesalt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph,prodrug or any combination thereof, in an amount effective to treatAR-positive and ER-positive refractory breast cancer in the subject. Inone embodiment, the subject is a female subject. In another embodiment,the subject is a male subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from AR-positive and ER-negative breastcancer, comprising the step of administering to the subject a selectiveandrogen receptor modulator of formulas I-XIV of this invention and/orits analog, derivative, isomer, metabolite, pharmaceutically acceptablesalt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph,prodrug or any combination thereof, in an amount effective to treatAR-positive and ER-negative metastatic breast cancer in the subject. Inone embodiment, the subject is a female subject. In another embodiment,the subject is a male subject.

In another embodiment of the present invention, a method is provided forto treating a subject suffering from triple negative breast cancer,comprising the step of administering to the subject a selective androgenreceptor modulator of formulas I-XIV of this invention and/or itsanalog, derivative, isomer, metabolite, pharmaceutically acceptablesalt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph,prodrug or any combination thereof, in an amount effective to treattriple negative breast cancer in the subject. In one embodiment, thesubject is a female subject. In another embodiment, the subject is amale subject.

In another embodiment of the present invention, a method is provided fortreating a subject suffering from breast cancer that has failed SERM(tamoxifen, toremifene), aromatase inhibitor, trastuzumab (Herceptin,ado-trastuzumab emtansine), pertuzumab (Perjeta), lapatinib, exemestane(Aromasin), bevacizumab (Avastin), and/or fulvestrant treatments,comprising the step of administering to the subject a selective androgenreceptor modulator of formulas I-XIV of this invention and/or itsanalog, derivative, isomer, metabolite, pharmaceutically acceptablesalt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph,prodrug or any combination thereof, in an amount effective to treatbreast cancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatments in the subject. In oneembodiment, the subject is a female subject. In another embodiment, thesubject is a male subject.

In another embodiment of the present invention, a method is provided fortreating, preventing, suppressing or inhibiting metastasis in a subjectsuffering from breast cancer, comprising the step of administering tothe subject a selective androgen receptor modulator of formulas I-XIV ofthis invention and/or its analog, derivative, isomer, metabolite,pharmaceutically acceptable salt, pharmaceutical product, hydrate,N-oxide, crystal, polymorph, prodrug or any combination thereof, in anamount effective to treat, prevent, suppress or inhibit metastasis inthe subject. In one embodiment, the subject is a female subject. Inanother embodiment, the subject is a male subject.

In another embodiment of the present invention, a method is provided fortreating and/or preventing skeletal related events in a subjectsuffering, comprising the step of administering to the subject aselective androgen receptor modulator of formulas I-XIV of thisinvention and/or its analog, derivative, isomer, metabolite,pharmaceutically acceptable salt, pharmaceutical product, hydrate,N-oxide, crystal, polymorph, prodrug or any combination thereof, in anamount effective to treat and/or prevent skeletal related events in thesubject. In one embodiment, the subject is a female subject. In anotherembodiment, the subject is a male subject.

In another embodiment of the present invention, a method is provided forimproving libido in a subject, comprising the step of administering tothe subject a selective androgen receptor modulator of formulas I-XIV ofthis invention and/or its analog, derivative, isomer, metabolite,pharmaceutically acceptable salt, pharmaceutical product, hydrate,N-oxide, crystal, polymorph, prodrug or any combination thereof, in anamount effective to improve libido in the subject. In one embodiment,the subject is a female subject. In another embodiment, the subject is amale subject.

In another embodiment of the present invention, a method is provided forimproving quality of life in a subject, comprising the step ofadministering to the subject a selective androgen receptor modulator offormulas I-XIV of this invention and/or its analog, derivative, isomer,metabolite, pharmaceutically acceptable salt, pharmaceutical product,hydrate, N-oxide, crystal, polymorph, prodrug or any combinationthereof, in an amount effective to quality of life in the subject. Inone embodiment, the subject is a female subject. In another embodiment,the subject is a male subject.

In another embodiment of the present invention, a method is provided fortreating, preventing, suppressing or inhibiting metastasis in a subjectsuffering from breast cancer, comprising the step of administering tothe subject a selective androgen receptor modulator of formulas I-XIV ofthis invention and/or its analog, derivative, isomer, metabolite,pharmaceutically acceptable salt, pharmaceutical product, hydrate,N-oxide, crystal, polymorph, prodrug or any combination thereof, in anamount effective to treat, prevent, suppress or inhibit metastasis inthe subject. In one embodiment, the subject is a female subject. Inanother embodiment, the subject is a male subject.

The substituent R is defined herein as an alkyl, haloalkyl, dihaloalkyl,trihaloalkyl, CH₂F, CHF₂, CF₃, CF₂CF₃; aryl, phenyl, halogen, alkenyl,or hydroxyl (OH).

An “alkyl” group refers to a saturated aliphatic hydrocarbon, includingstraight-chain, branched-chain and cyclic alkyl groups. In oneembodiment, the alkyl group has 1-12 carbons. In another embodiment, thealkyl group has 1-7 carbons. In another embodiment, the alkyl group has1-6 carbons. In another embodiment, the alkyl group has 1-4 carbons. Thealkyl group may be unsubstituted or substituted by one or more groupsselected from halogen, hydroxy, alkoxy carbonyl, amido, alkylamido,dialkylamido, nitro, amino, alkylamino, dialkylamino, carboxyl, thio andthioalkyl.

A “haloalkyl” group refers to an alkyl group as defined above, which issubstituted by one or more halogen atoms, e.g. by F, Cl, Br or I.

An “aryl” group refers to an aromatic group having at least onecarbocyclic aromatic group or heterocyclic aromatic group, which may beunsubstituted or substituted by one or more groups selected fromhalogen, haloalkyl, hydroxy, alkoxy carbonyl, amido, alkylamido,dialkylamido, nitro, amino, alkylamino, dialkylamino, carboxy or thio orthioalkyl. Nonlimiting examples of aryl rings are phenyl, naphthyl,pyranyl, pyrrolyl, pyrazinyl, pyrimidinyl, pyrazolyl, pyridinyl,furanyl, thiophenyl, thiazolyl, imidazolyl, isoxazolyl, and the like.

A “hydroxyl” group refers to an OH group. An “alkenyl” group refers to agroup having at least one carbon to carbon double bond. A halo grouprefers to F, Cl, Br or I.

An “arylalkyl” group refers to an alkyl bound to an aryl, wherein alkyland aryl are as defined above. An example of an aralkyl group is abenzyl group.

Biological Activity of Selective Androgen Receptor Modulators

The selective androgen receptor modulators provided herein are a newclass of compounds, which suppress growth of AR-positive breast cancers.The compounds of this invention have a tissue-selective myoanabolicactivity profile of a nonsteroidal ligand for the androgen receptor.Furthermore compounds of the present invention are non-aromatizable,non-virilizing, and are not commonly cross-reactive with ER and PR. Inaddition, in one embodiment, the selective androgen receptor modulators(SARMs) of the present invention are beneficial to refractory breastcancer patients undergoing chemotherapy due to anabolism.

As contemplated herein, the appropriately substituted selective androgenreceptor modulators of the present invention are useful for: a) treatinga subject suffering from breast cancer; b) treating a subject sufferingfrom metastatic breast cancer; c) treating a subject suffering fromrefractory breast cancer; d) treating a subject suffering fromAR-positive breast cancer; e) treating a subject suffering fromAR-positive refractory breast cancer; f) treating a subject sufferingfrom AR-positive metastatic breast cancer; g) treating a subjectsuffering from AR-positive and ER-positive breast cancer; h) treating asubject suffering from AR-positive breast cancer with or withoutexpression of ER, PR, and/or HER2; i) treating a subject suffering fromtriple negative breast cancer; j) treating a subject suffering fromadvanced breast cancer; k) treating a subject suffering from breastcancer that has failed SERM (tamoxifen, toremifene), aromataseinhibitor, trastuzumab (Herceptin, ado-trastuzumab emtansine),pertuzumab (Perjeta), lapatinib, exemestane (Aromasin), bevacizumab(Avastin), and/or fulvestrant treatments; l) treating a subjectsuffering from ER positive breast cancer; m) treating, preventing,suppressing or inhibiting metastasis in a subject suffering from breastcancer; n) prolonging survival of a subject with breast cancer; o)slowing the progression of breast cancer in a subject; and/or p)prolonging the progression-free survival of a subject with breastcancer.

In one embodiment, a “refractory breast cancer” is a breast cancer thathas not responded to treatment. In another embodiment, a “refractorybreast cancer” is a breast cancer resistant to treatment. In oneembodiment, refractory breast cancer is refractory metastatic breastcancer. In one embodiment, refractory breast cancer has not responded totreatment with anthracyclines, taxanes, capecitabine, ixabepilone, SERM(tamoxifen, toremifene), aromatase inhibitor, trastuzumab (Herceptin,ado-trastuzumab emtansine), pertuzumab (Perjeta), lapatinib, exemestane(Aromasin), bevacizumab (Avastin), fulvestrant or any combinationthereof.

In one embodiment, a “triple negative breast cancer” is defined by lackof expression of estrogen, progesterone, and ErbB2 (also known as humanepidermal growth factor receptor 2 (HER2)) receptors. This subgroupaccounts for 15% of all types of breast cancer. This subtype of breastcancer is clinically characterized as more aggressive and lessresponsive to standard treatment and associated with poorer overallpatient prognosis.

In one embodiment, the methods of this invention are directed totreating a subject suffering from AR-positive breast cancer, regardlessof grade, stage or prior treatments.

In one embodiment, the methods of this invention are first, second,third, or fourth line therapies for breast cancer. A first line therapyrefers to a medical therapy recommended for the initial treatment of adisease, sign or symptom. A second line therapy therapy is given wheninitial treatment (first-line therapy) does not work, or stops working.Third line therapy is given when both initial treatment (first-linetherapy) and subsequent treatment (second-line therapy) does not work,or stop working, etc.

As used herein, “kinases” are a group of enzymes that catalyze thetransfer of a phosphate group from a donor, such as ADP or ATP, to anacceptor. In one embodiment, phosphorylation results in a functionalchange of the target protein (substrate) by changing enzyme activity,cellular location, or association with other proteins kinases. Kinasesregulate the majority of cellular pathways, especially those involved insignal transduction. In one embodiment, deregulated kinase activity is afrequent cause of disease, in particular cancer, wherein kinasesregulate many aspects that control cell growth, movement and death. Inone embodiment, drugs that inhibit specific kinases are used to treatkinase-related diseases, including cancer. In one embodiment, HER2positive breast cancers are susceptible to HER2 kinase inhibitors (e.g.,trastuzumab and lapatinib) and are generally used in metastatic disease.However, some breast cancers are refractory to HER2 kinase inhibitortreatment.

As used herein, receptors for extracellular signaling molecules arecollectively referred to as “cell signaling receptors”. Many cellsignaling receptors are transmembrane proteins on a cell surface; whenthey bind an extracellular signaling molecule (i.e., a ligand), theybecome activated so as to generate a cascade of intracellular signalsthat alter the behavior of the cell. In contrast, in some cases, thereceptors are inside the cell and the signaling ligand has to enter thecell to activate them; these signaling molecules therefore must besufficiently small and hydrophobic to diffuse across the plasma membraneof the cell.

Steroid hormones are one example of small hydrophobic molecules thatdiffuse directly across the plasma membrane of target cells and bind tointracellular cell signaling receptors. These receptors are structurallyrelated and constitute the intracellular receptor superfamily (orsteroid-hormone receptor superfamily). Steroid hormone receptors includebut are not limited to progesterone receptors, estrogen receptors,androgen receptors, glucocorticoid receptors, and mineralocorticoidreceptors. In one embodiment, the present invention is directed toandrogen receptors. In one embodiment, the present invention is directedto androgen receptor agonists. In one embodiment, the present inventionis directed to progesterone receptors. In one embodiment, the presentinvention is directed to progesterone receptor antagonists.

In addition to ligand binding to the receptors, the receptors can beblocked to prevent ligand binding. When a substance binds to a receptor,the three-dimensional structure of the substance fits into a spacecreated by the three-dimensional structure of the receptor in a ball andsocket configuration. The better the ball fits into the socket, the moretightly it is held. This phenomenon is called affinity. If the affinityof a substance is greater than the original hormone, it will competewith the hormone and bind the binding site more frequently. Once bound,signals may be sent through the receptor into the cells, causing thecell to respond in some fashion. This is called activation. Onactivation, the activated receptor then directly regulates thetranscription of specific genes. But the substance and the receptor mayhave certain attributes, other than affinity, in order to activate thecell. Chemical bonds between atoms of the substance and the atoms of thereceptors may form. In some cases, this leads to a change in theconfiguration of the receptor, which is enough to begin the activationprocess (called signal transduction).

In one embodiment, the compounds of this invention inhibit theintratumoral expression of genes and pathways that promote breast cancerdevelopment through their actions on the AR. In one embodiment, acompound of this invention inhibits intratumoral expression of Muc1,SLUG, VCAM1, SPARC or MMP2, or any combination thereof. In anotherembodiment, Compound VIII inhibits gene expression that promotes breastcancer.

In one embodiment, a receptor antagonist is a substance which bindsreceptors and inactivates them. In one embodiment, a selective androgenreceptor modulator is a molecule that exhibits in vivo tissueselectivity, activating signaling activity of the androgen receptor (AR)in anabolic (muscle, bone, etc.) tissues to a greater extent than in theandrogenic tissues. Thus, in one embodiment, the selective androgenreceptor modulators of the present invention are useful in binding toand activating steroidal hormone receptors. In one embodiment, the SARMcompound of the present invention is an agonist which binds the androgenreceptor. In another embodiment, the compound has high affinity for theandrogen receptor.

Assays to determine whether the compounds of the present invention areAR agonists or antagonists are well known to a person skilled in theart. For example, AR agonistic activity can be determined by monitoringthe ability of the selective androgen receptor modulators to maintainand/or stimulate the growth of AR containing androgenic tissue such asprostate and seminal vesicles, as measured by weight, in castratedanimals. AR antagonistic activity can be determined by monitoring theability of the selective androgen receptor modulators to inhibit thegrowth of AR containing tissue in intact animals or counter the effectsof testosterone in castrated animals.

An androgen receptor (AR) is an androgen receptor of any species, forexample a mammal. In one embodiment, the androgen receptor is anandrogen receptor of a human. Thus, in another embodiment, the selectiveandrogen receptor modulators bind reversibly to an androgen receptor ofa human. In another embodiment, the selective androgen receptormodulators bind reversibly to an androgen receptor of a mammal.

As contemplated herein, the term “selective androgen receptor modulator”(SARM) refers to, in one embodiment, a molecule that exhibits in vivotissue selectivity, activating signaling activity of the AndrogenReceptor in anabolic (muscle, bone, etc.) tissues to a greater extentthan in the androgenic tissues. In another embodiment, a selectiveandrogen receptor modulator selectively binds the androgen receptor. Inanother embodiment, a selective androgen receptor modulator selectivelyaffects signaling through the androgen receptor. In one embodiment, theSARM is a partial agonist. In one embodiment, the SARM is atissue-selective agonist, or in some embodiments, a tissue-selectiveantagonist.

In one embodiment, a SARM of this invention exerts its effects on theandrogen receptor in a tissue-dependent manner. In one embodiment, aSARM of this to invention will have an IC₅₀ or EC₅₀ with respect to AR,as determined using AR transactivation assays, as known in the art, or,in other embodiments, as described herein.

The term “IC₅₀” refers, in some embodiments, to a concentration of theSARM which reduces the activity of a target (e.g., AR) to half-maximallevel.

The term “EC₅₀” refers, in some embodiments, to a concentration of theSARM that produces a half-maximal effect.

For example, utilizing transactivation assays, FIG. 5 shows thatcompounds of this invention exhibit AR agonist activity in MDA-MB-231cells transfected with AR.

As defined herein, “contacting” means that the selective androgenreceptor modulators of the present invention are introduced into asample containing the enzyme in a test tube, flask, tissue culture,chip, array, plate, microplate, capillary, or the like, and incubated ata temperature and time sufficient to permit binding of the selectiveandrogen receptor modulators to the receptor. Methods for contacting thesamples with the selective androgen receptor modulators or otherspecific binding components are known to those skilled in the art andmay be selected depending on the type of assay protocol to be run.Incubation methods are also standard and are known to those skilled inthe art.

In another embodiment, the term “contacting” means that the selectiveandrogen receptor modulators of the present invention are introducedinto a subject receiving treatment, and the selective androgen receptormodulator is allowed to come in contact with the androgen receptor invivo.

As used herein, the term “treating” includes preventative as well asdisorder remitative treatment. As used herein, the terms “reducing”,“suppressing” and “inhibiting” have their commonly understood meaning oflessening or decreasing. As used herein, the term “progression” meansincreasing in scope or severity, advancing, growing or becoming worse.As used herein, the term “recurrence” means the return of a diseaseafter a remission. As used herein, the term “delaying” means stopping,hindering, slowing down, postponing, holding up or setting back. As usedherein, the term “metastasis” refers to the transfer of a disease fromone organ or part thereof to another not directly connected with it.Metastasis can occur for example as a result of transfer of malignantcells from one organ (for example breast) to other organs.

In one embodiment, “treating” refers to reducing tumor growth by 75%, asdemonstrated in Example 8. In another embodiment, treating refers toreducing tumor growth by at least 75%. In another embodiment, treatingrefers to reducing tumor growth by at least 50%. In another embodiment,treating refers to reducing tumor growth by at least 25%. In anotherembodiment, treating refers to reducing tumor growth by 50-100%. Inanother embodiment, treating refers to reducing tumor growth by 70-80%.In another embodiment, treating refers to reducing tumor growth by25-125%.

In another embodiment, “treating” refers to reducing tumor weight by50%, as demonstrated in Example 8. In another embodiment, treatingrefers to reducing tumor weight by at least 50%. In another embodiment,treating refers to reducing tumor weight by at least 40%. In anotherembodiment, treating refers to reducing tumor weight by at least 30%. Inanother embodiment, treating refers to reducing tumor weight by at least20%. In another embodiment, treating refers to reducing tumor growth by25-75%. In another embodiment, treating refers to reducing tumor growthby 25-100%.

As used herein, the term “administering” refers to bringing a subject incontact with a compound of the present invention. As used herein,administration can be accomplished in vitro, i.e. in a test tube, or invivo, i.e. in cells or tissues of living organisms, for example humans.In one embodiment, the present invention encompasses administering thecompounds of the present invention to a subject.

In one embodiment, a compound of the present invention is administeredto a subject once a week. In another embodiment, a compound of thepresent invention is administered to a subject twice a week. In anotherembodiment, a compound of the present invention is administered to asubject three times a week. In another embodiment, a compound of thepresent invention is administered to a subject four times a week. Inanother embodiment, a compound of the present invention is administeredto a subject five times a week. In another embodiment, a compound of thepresent invention is administered to a subject daily. In anotherembodiment, a compound of the present invention is administered to asubject weekly. In another embodiment, a compound of the presentinvention is administered to a subject bi-weekly. In another embodiment,a to compound of the present invention is administered to a subjectmonthly.

In one embodiment, the methods of the present invention compriseadministering a selective androgen receptor modulator as the sole activeingredient. However, also encompassed within the scope of the presentinvention are methods for hormone therapy, for treating breast cancer,for delaying the progression of breast cancer, and for preventing andtreating the recurrence of breast cancer and/or breast cancermetastasis, which comprise administering the selective androgen receptormodulators in combination with one or more therapeutic agents. Theseagents include, but are not limited to: selective estrogen receptormodulators (SERM), selective estrogen receptor degraders (fulvestrant),HER2 inhibitors (lapatinib, trastuzumab), bevacizumab, chemotherapeuticagents, taxanes, anthracyclines, epothilones, LHRH analogs, reversibleantiandrogens, antiestrogens, anticancer drugs, 5-alpha reductaseinhibitors, aromatase inhibitors (exemestane, anastrozole, letrozole,vorozole, formestane, fadrozole), progestins, agents acting throughother nuclear hormone receptors such as progesterone and estrogenreceptors, estrogens, progestins, PDE5 inhibitors, apomorphine,bisphosphonate, growth factor inhibitors (such as those that inhibitVEGF, IGF and the like), or one or more additional selective androgenreceptor modulators (SARMs).

Additional therapeutic agents that may be administered in combinationwith a selective androgen receptor modulator compound of this inventioninclude, but are not limited to: Abitrexate (R)(methotrexate), Abraxane(paclitaxel albumin-stabilized nanoparticle formulation),ado-trastuzumab emtansine, adriamycin PFS (doxorubicin hydrochloride),adriamycin RDF (doxorubicin hydrochloride), Adrucil (fluorouracil),Afinitor (everolimus), anastrozole, Arimidex (anastrozole), Aromasin(exemestane), capecitabine, Clafen (cyclophosphamide), cyclophosphamide,Cytoxan (cyclophosphamide), docetaxel, doxorubicin hydrochloride, Efudex(fluorouracil), Ellence (epirubicin hydrochloride), epirubicinhydrochloride, everolimus, exemestane, Fareston (toremifene), Faslodex(fulvestrant), Femara (letrozole), Fluoroplex (fluorouracil),fluorouracil, Folex (methotrexate), Folex PFS (methotrexate),fulvestrant, gemcitabine hydrochloride, Gemzar (gemcitabinehydrochloride), Herceptin (trastuzumab), ixabepilone, Ixempra(ixabepilone), lapatinib ditosylate, letrozole, methotrexate,methotrexate LPF (methotrexate), Mexate (methotrexate), Mexate-AQ to(methotrexate), Neosar (cyclophosphamide), Nolvadex (tamoxifen citrate),paclitaxel, paclitaxel albumin-stabilized nanoparticle formulation,Perjeta (pertuzumab), pertuzumab, yamoxifen citrate, Taxol (paclitaxel),Taxotere (docetaxel), trastuzumab, toremifene, Tykerb (lapatinibditosylate), Xeloda (capecitabine).

Thus, in one embodiment, the methods of the present invention compriseadministering the selective androgen receptor modulator, in combinationwith a selective estrogen receptor modulator. Thus, in one embodiment,the methods of the present invention comprise administering theselective androgen receptor modulator, in combination with a selectiveestrogen receptor degrader (fluvestrant). Thus, in one embodiment, themethods of the present invention comprise administering the selectiveandrogen receptor modulator, in combination with a HER2 inhibitor(lapatinib, trastuzumab). Thus, in one embodiment, the methods of thepresent invention comprise administering the selective androgen receptormodulator, in combination with a VEGF-A inhibitor (bevacizumab). Thus,in one embodiment, the methods of the present invention compriseadministering the selective androgen receptor modulator, in combinationwith a chemotherapeutic agent. In one embodiment, the chemotherapeuticagent is a taxane. In another embodiment, the chemotherapeutic agent isan anthracycline. In one embodiment, the chemotherapeutic agent is anepothilone (ixabepilone). Thus, in one embodiment, the methods of thepresent invention comprise administering the selective androgen receptormodulator, in combination with an LHRH analog. In another embodiment,the methods of the present invention comprise administering a selectiveandrogen receptor modulator, in combination with a reversibleantiandrogen. In another embodiment, the methods of the presentinvention comprise administering a selective androgen receptormodulator, in combination with an antiestrogen. In another embodiment,the methods of the present invention comprise administering a selectiveandrogen receptor modulator, in combination with an anticancer drug. Inanother embodiment, the methods of the present invention compriseadministering a selective androgen receptor modulator, in combinationwith a 5-alpha reductase inhibitor. In another embodiment, the methodsof the present invention comprise administering a selective androgenreceptor modulator of this invention, in combination with an aromataseinhibitor. In another embodiment, the methods of the present inventioncomprise administering a selective androgen receptor modulator of thisinvention, in combination with a progestin. In another embodiment, themethods of the present invention comprise administering a selectiveandrogen receptor modulator of this invention, in combination with anagent acting through other nuclear hormone receptors. In anotherembodiment, the methods of the present invention comprise administeringa selective androgen receptor modulator of this invention, incombination with a selective estrogen receptor modulators (SERM). Inanother embodiment, the methods of the present invention compriseadministering a selective androgen receptor modulator of this invention,in combination with a progestin or anti-progestin. In anotherembodiment, the methods of the present invention comprise administeringa selective androgen receptor modulator, in combination with anestrogen. In another embodiment, the methods of the present inventioncomprise administering a selective androgen receptor modulator of thisinvention, in combination with a PDES inhibitor. In another embodiment,the methods of the present invention comprise administering a selectiveandrogen receptor modulator of this invention, in combination withapomorphine. In another embodiment, the methods of the present inventioncomprise administering a selective androgen receptor modulator of thisinvention, in combination with a bisphosphonate. In another embodiment,the methods of the present invention comprise administering a selectiveandrogen receptor modulator of this invention, in combination with agrowth factor inhibitor. In another embodiment, the methods of thepresent invention comprise administering a selective androgen receptormodulator of this invention, in combination with one or more additionalselective androgen receptor modulators (SARMs).

In another embodiment, the methods of the present invention compriseadministering a selective androgen receptor modulator of this invention,in combination with Abitrexate (methotrexate). In another embodiment,the methods of the present invention comprise administering a selectiveandrogen receptor modulator of this invention, in combination withAbraxane (paclitaxel albumin-stabilized nanoparticle formulation). Inanother embodiment, the methods of the present invention compriseadministering a selective androgen receptor modulator of this invention,in combination with ado-trastuzumab emtansine. In another embodiment,the methods of the present invention comprise administering a selectiveandrogen receptor modulator of this invention, in combination withAdriamycin PFS (doxorubicin hydrochloride). In another embodiment, themethods of the present invention comprise administering a selective toandrogen receptor modulator of this invention, in combination withAdriamycin RDF (doxorubicin hydrochloride). In another embodiment, themethods of the present invention comprise administering a selectiveandrogen receptor modulator of this invention, in combination withAdrucil (fluorouracil). In another embodiment, the methods of thepresent invention comprise administering a selective androgen receptormodulator of this invention, in combination with Afinitor (everolimus).In another embodiment, the methods of the present invention compriseadministering a selective androgen receptor modulator of this invention,in combination with anastrozole. In another embodiment, the methods ofthe present invention comprise administering a selective androgenreceptor modulator of this invention, in combination with Arimidex(anastrozole). In another embodiment, the methods of the presentinvention comprise administering a selective androgen receptor modulatorof this invention, in combination with Aromasin (exemestane). In anotherembodiment, the methods of the present invention comprise administeringa selective androgen receptor modulator of this invention, incombination with capecitabine. In another embodiment, the methods of thepresent invention comprise administering a selective androgen receptormodulator of this invention, in combination with Clafen(cyclophosphamide). In another embodiment, the methods of the presentinvention comprise administering a selective androgen receptor modulatorof this invention, in combination with cyclophosphamide. In anotherembodiment, the methods of the present invention comprise administeringa selective androgen receptor modulator of this invention, incombination with Cytoxan (cyclophosphamide). In another embodiment, themethods of the present invention comprise administering a selectiveandrogen receptor modulator of this invention, in combination withdocetaxel. In another embodiment, the methods of the present inventioncomprise administering a selective androgen receptor modulator of thisinvention, in combination with doxorubicin hydrochloride. In anotherembodiment, the methods of the present invention comprise administeringa selective androgen receptor modulator of this invention, incombination with Efudex (fluorouracil). In another embodiment, themethods of the present invention comprise administering a selectiveandrogen receptor modulator of this invention, in combination withEllence (epirubicin hydrochloride). In another embodiment, the methodsof the present invention comprise administering a selective androgenreceptor modulator of this invention, in combination with epirubicin tohydrochloride. In another embodiment, the methods of the presentinvention comprise administering a selective androgen receptor modulatorof this invention, in combination with everolimus. In anotherembodiment, the methods of the present invention comprise administeringa selective androgen receptor modulator of this invention, incombination with exemestane. In another embodiment, the methods of thepresent invention comprise administering a selective androgen receptormodulator of this invention, in combination with Fareston (toremifene).In another embodiment, the methods of the present invention compriseadministering a selective androgen receptor modulator of this invention,in combination with Faslodex (fulvestrant). In another embodiment, themethods of the present invention comprise administering a selectiveandrogen receptor modulator of this invention, in combination withFemara (letrozole). In another embodiment, the methods of the presentinvention comprise administering a selective androgen receptor modulatorof this invention, in combination with Fluoroplex (fluorouracil). Inanother embodiment, the methods of the present invention compriseadministering a selective androgen receptor modulator of this invention,in combination with fluorouracil. In another embodiment, the methods ofthe present invention comprise administering a selective androgenreceptor modulator of this invention, in combination with Folex(methotrexate). In another embodiment, the methods of the presentinvention comprise administering a selective androgen receptor modulatorof this invention, in combination with Folex PFS (methotrexate). Inanother embodiment, the methods of the present invention compriseadministering a selective androgen receptor modulator of this invention,in combination with fulvestrant. In another embodiment, the methods ofthe present invention comprise administering a selective androgenreceptor modulator of this invention, in combination with gemcitabinehydrochloride. In another embodiment, the methods of the presentinvention comprise administering a selective androgen receptor modulatorof this invention, in combination with Gemzar (gemcitabinehydrochloride). In another embodiment, the methods of the presentinvention comprise administering a selective androgen receptor modulatorof this invention, in combination with Herceptin (trastuzumab). Inanother embodiment, the methods of the present invention compriseadministering a selective androgen receptor modulator of this invention,in combination with ixabepilone. In another embodiment, the methods ofthe present invention comprise administering a selective androgenreceptor modulator of this invention, in combination with Ixempra(ixabepilone). In another embodiment, the methods of the presentinvention comprise administering a selective androgen receptor modulatorof this invention, in combination with lapatinib ditosylate. In anotherembodiment, the methods of the present invention comprise administeringa selective androgen receptor modulator of this invention, incombination with letrozole. In another embodiment, the methods of thepresent invention comprise administering a selective androgen receptormodulator of this invention, in combination with methotrexate. Inanother embodiment, the methods of the present invention compriseadministering a selective androgen receptor modulator of this invention,in combination with methotrexate LPF (methotrexate). In anotherembodiment, the methods of the present invention comprise administeringa selective androgen receptor modulator of this invention, incombination with Mexate (methotrexate). In another embodiment, themethods of the present invention comprise administering a selectiveandrogen receptor modulator of this invention, in combination withMexate-AQ (methotrexate). In another embodiment, the methods of thepresent invention comprise administering a selective androgen receptormodulator of this invention, in combination with Neosar(cyclophosphamide). In another embodiment, the methods of the presentinvention comprise administering a selective androgen receptor modulatorof this invention, in combination with Nolvadex (tamoxifen citrate). Inanother embodiment, the methods of the present invention compriseadministering a selective androgen receptor modulator of this invention,in combination with paclitaxel. In another embodiment, the methods ofthe present invention comprise administering a selective androgenreceptor modulator of this invention, in combination with paclitaxelalbumin-stabilized nanoparticle formulation. In another embodiment, themethods of the present invention comprise administering a selectiveandrogen receptor modulator of this invention, in combination withPerjeta (pertuzumab). In another embodiment, the methods of the presentinvention comprise administering a selective androgen receptor modulatorof this invention, in combination with pertuzumab. In anotherembodiment, the methods of the present invention comprise administeringa selective androgen receptor modulator of this invention, incombination with tamoxifen citrate. In another embodiment, the methodsof the present invention comprise administering a selective androgenreceptor modulator of this invention, in combination with Taxol(paclitaxel). In another embodiment, the methods of the presentinvention comprise administering a selective androgen receptor modulatorof this invention, in combination with Taxotere (docetaxel). In anotherembodiment, the methods of the present invention comprise administeringa selective androgen receptor modulator of this invention, incombination with trastuzumab. In another embodiment, the methods of thepresent invention comprise administering a selective androgen receptormodulator of this invention, in combination with oremifene. In anotherembodiment, the methods of the present invention comprise administeringa selective androgen receptor modulator of this invention, incombination with Tykerb (lapatinib ditosylate). In another embodiment,the methods of the present invention comprise administering a selectiveandrogen receptor modulator of this invention, in combination withXeloda (capecitabine).

In one embodiment, the methods of the present invention compriseadministering a pharmaceutical composition (or pharmaceuticalpreparation, used herein interchangeably) comprising the selectiveandrogen receptor modulator of the present invention and/or its analog,derivative, isomer, metabolite, pharmaceutical product, hydrate,N-oxide, polymorph, crystal, prodrug or any combination thereof; and asuitable carrier or diluent.

Pharmaceutical Compositions:

As used herein, “pharmaceutical composition” means therapeuticallyeffective amounts of the selective androgen receptor modulator togetherwith suitable diluents, preservatives, solubilizers, emulsifiers,adjuvant and/or carriers. A “therapeutically effective amount” as usedherein refers to that amount which provides a therapeutic effect for agiven condition and administration regimen. Such compositions areliquids or lyophilized or otherwise dried formulations and includediluents of various buffer content (e.g., Tris-HCI, acetate, phosphate),pH and ionic strength, additives such as albumin or gelatin to preventabsorption to surfaces, detergents (e.g., Tween 20, Tween 80, PluronicF68, bile acid salts), solubilizing agents (e.g., glycerol, polyethyleneglycerol), anti-oxidants (e.g., ascorbic acid, sodium metabisulfite),preservatives (e.g., Thimerosal, benzyl alcohol, parabens), bulkingsubstances or tonicity modifiers (e.g., lactose, mannitol), covalentattachment of polymers such as polyethylene glycol to the protein,complexation with metal ions, or incorporation of the material into oronto particulate preparations of polymeric compounds such as polylacticacid, polglycolic acid, hydrogels, etc, or onto liposomes,microemulsions, micelles, unilamellar or multilamellar vesicles,erythrocyte ghosts, or spheroplasts). Such compositions will influencethe physical state, solubility, stability, rate of in vivo release, andrate of in vivo clearance. Controlled or sustained release compositionsinclude formulation in lipophilic depots (e.g., fatty acids, waxes,oils).

Also comprehended by the invention are particulate compositions coatedwith polymers (e.g., poloxamers or poloxamines). Other embodiments ofthe compositions of the invention incorporate particulate formsprotective coatings, protease inhibitors or permeation enhancers forvarious routes of administration, including parenteral, pulmonary, nasaland oral. In one embodiment the pharmaceutical composition isadministered parenterally, paracancerally, transmucosally,transdermally, intramuscularly, intravenously, intradermally,subcutaneously, intraperitoneally, intraventricularly, intravaginally,intracranially and intratumorally.

Further, as used herein “pharmaceutically acceptable carriers” are wellknown to those skilled in the art and include, but are not limited to,0.01-0.1 M and preferably 0.05 M phosphate buffer or about 0.8% saline.Additionally, such pharmaceutically acceptable carriers may be aqueousor non-aqueous solutions, suspensions, and emulsions. Examples ofnon-aqueous solvents are propylene glycol, polyethylene glycol,vegetable oils such as olive oil, and injectable organic esters such asethyl oleate. Aqueous carriers include water, alcoholic/aqueoussolutions, emulsions or suspensions, including saline and bufferedmedia.

Parenteral vehicles include sodium chloride solution, Ringer's dextrose,dextrose and sodium chloride, lactated Ringer's and fixed oils.Intravenous vehicles include fluid and nutrient replenishers,electrolyte replenishers such as those based on Ringer's dextrose, andthe like. Preservatives and other additives may also be present, suchas, for example, antimicrobials, antioxidants, collating agents, inertgases and the like.

Controlled or sustained release compositions include formulation inlipophilic depots (e.g. fatty acids, waxes, oils). Also comprehended bythe invention are particulate compositions coated with polymers (e.g.poloxamers or poloxamines) and the compound coupled to antibodiesdirected against tissue-specific receptors, ligands or antigens orcoupled to ligands of tissue-specific receptors.

Other embodiments of the compositions of the invention incorporateparticulate forms, protective coatings, protease inhibitors orpermeation enhancers for various routes of administration, includingparenteral, pulmonary, nasal and oral.

Compounds modified by the covalent attachment of water-soluble polymerssuch as polyethylene glycol, copolymers of polyethylene glycol andpolypropylene glycol, carboxymethyl cellulose, dextran, polyvinylalcohol, polyvinylpyrrolidone or polyproline are known to exhibitsubstantially longer half-lives in blood following intravenous injectionthan do the corresponding unmodified compounds (Abuchowski et al., 1981;Newmark et al., 1982; and Katre et al., 1987). Such modifications mayalso increase the compound's solubility in aqueous solution, eliminateaggregation, enhance the physical and chemical stability of thecompound, and greatly reduce the immunogenicity and reactivity of thecompound. As a result, the desired in vivo biological activity may beachieved by the administration of such polymer-compound abducts lessfrequently or in lower doses than with the unmodified compound.

In yet another embodiment, the pharmaceutical composition can bedelivered in a controlled release system. For example, the agent may beadministered using intravenous infusion, an implantable osmotic pump, atransdermal patch, liposomes, or other modes of administration. In oneembodiment, a pump may be used (see Langer, supra; Sefton, CRC Crit.Ref. Biomed. Eng. 14:201 (1987); Buchwald et al., Surgery 88:507 (1980);Saudek et al., N. Engl. J. Med. 321:574 (1989). In another embodiment,polymeric materials can be used. In yet another embodiment, a controlledrelease system can be placed in proximity to the therapeutic target,i.e., the brain, thus requiring only a fraction of the systemic dose(see, e.g., Goodson, in Medical Applications of Controlled Release,supra, vol. 2, pp. 115-138 (1984). Other controlled release systems arediscussed in the review by Langer (Science 249:1527-1533 (1990).

The pharmaceutical preparation can comprise the selective androgenreceptor modulator alone, or can further include a pharmaceuticallyacceptable carrier, and can be in solid or liquid form such as tablets,powders, capsules, pellets, solutions, suspensions, elixirs, emulsions,gels, creams, or suppositories, including rectal and urethralsuppositories. Pharmaceutically acceptable carriers include gums,starches, sugars, cellulosic materials, and mixtures thereof. Thepharmaceutical preparation containing the selective androgen receptormodulator can be administered to a subject by, for example, subcutaneousimplantation of a pellet; in a further embodiment, the pellet providesfor controlled release of selective androgen receptor modulator over aperiod of time. The preparation can also be administered by intravenous,intraarterial, or intramuscular injection of a liquid preparation, oraladministration of a liquid or solid preparation, or by topicalapplication. Administration can also be accomplished by use of a rectalsuppository or a urethral suppository.

The pharmaceutical preparations of the invention can be prepared byknown dissolving, mixing, granulating, or tablet-forming processes. Fororal administration, the selective androgen receptor modulators or theirphysiologically tolerated derivatives such as salts, esters, N-oxides,and the like are mixed with additives customary for this purpose, suchas vehicles, stabilizers, or inert diluents, and converted by customarymethods into suitable forms for administration, such as tablets, coatedtablets, hard or soft gelatin capsules, aqueous, alcoholic or oilysolutions. Examples of suitable inert vehicles are conventional tabletbases such as lactose, sucrose, or cornstarch in combination withbinders such as acacia, cornstarch, gelatin, with disintegrating agentssuch as cornstarch, potato starch, alginic acid, or with a lubricantsuch as stearic acid or magnesium stearate.

Examples of suitable oily vehicles or solvents are vegetable or animaloils such as sunflower oil or fish-liver oil. Preparations can beeffected both as dry and as wet granules. For parenteral administration(subcutaneous, intravenous, intraarterial, or intramuscular injection),the selective androgen receptor modulators or their physiologicallytolerated derivatives such as salts, esters, N-oxides, and the like areconverted into a solution, suspension, or emulsion, if desired with thesubstances customary and suitable for this purpose, for example,solubilizers or other auxiliaries. Examples are sterile liquids such aswater and oils, with or without the addition of a surfactant and otherpharmaceutically acceptable adjuvants. Illustrative oils are those ofpetroleum, animal, vegetable, or synthetic origin, for example, peanutoil, soybean oil, or mineral oil. In general, water, saline, aqueousdextrose and related sugar solutions, and glycols such as propyleneglycols or polyethylene glycol are preferred liquid carriers,particularly for injectable solutions.

The preparation of pharmaceutical compositions which contain an activecomponent is well understood in the art. Such compositions can beprepared as aerosols of the active component delivered to thenasopharynx or as injectables, either as liquid solutions orsuspensions; however, solid forms suitable for solution in, orsuspension in, liquid prior to injection can also be prepared. Thepreparation can also be emulsified. The active therapeutic ingredient isoften mixed with excipients which are pharmaceutically acceptable andcompatible with the active ingredient. Suitable excipients are, forexample, water, saline, dextrose, glycerol, ethanol, or the like or anycombination thereof.

In addition, the composition can contain minor amounts of auxiliarysubstances such as wetting or emulsifying agents, pH buffering agentswhich enhance the effectiveness of the active ingredient.

An active component can be formulated into the composition asneutralized pharmaceutically acceptable salt forms. Pharmaceuticallyacceptable salts include the acid addition salts (formed with the freeamino groups of the polypeptide or antibody molecule), which are formedwith inorganic acids such as, for example, hydrochloric or phosphoricacids, or such organic acids as acetic, oxalic, tartaric, mandelic, andthe like. Salts formed from the free carboxyl groups can also be derivedfrom inorganic bases such as, for example, sodium, potassium, ammonium,calcium, or ferric hydroxides, and such organic bases as isopropylamine,trimethylamine, 2-ethylamino ethanol, histidine, procaine, and the like.

For topical administration to body surfaces using, for example, creams,gels, drops, and the like, the selective androgen receptor modulators ortheir physiologically tolerated derivatives such as salts, esters,N-oxides, and the like are prepared and applied as solutions,suspensions, or emulsions in a physiologically acceptable diluent withor without a pharmaceutical carrier.

In another embodiment, the active compound can be delivered in avesicle, in particular a liposome (see Langer, Science 249:1527-1533(1990); Treat et al., in Liposomes in the Therapy of Infectious Diseaseand Cancer, Lopez-Berestein and Fidler (eds.), Liss, New York, pp.353-365 (1989); Lopez-Berestein, ibid., pp. 317-327; see generallyibid).

For use in medicine, the salts of the selective androgen receptormodulator will be pharmaceutically acceptable salts. Other salts may,however, be useful in the preparation of the compounds of the inventionor of their pharmaceutically acceptable salts. Suitable pharmaceuticallyacceptable salts of the compounds of this invention include acidaddition salts which may, for example, be formed by mixing a solution ofthe compound of the invention with a solution of a pharmaceuticallyacceptable acid such as hydrochloric acid, sulphuric acid,methanesulphonic acid, fumaric acid, maleic acid, succinic acid, aceticacid, benzoic: acid, oxalic acid, citric acid, tartaric acid, carbonicacid or phosphoric acid.

In one embodiment, the term “about”, refers to a deviance of between0.0001-5% from the indicated number or range of numbers. In oneembodiment, the term “about”, refers to a deviance of between 1-10% fromthe indicated number or range of numbers. In one embodiment, the term“about”, refers to a deviance of up to 25% from the indicated number orrange of numbers.

In some embodiments, the term “comprise” or grammatical forms thereof,refers to the inclusion of the indicated active agent, such as thecompound of this invention, as well as inclusion of other active agents,and pharmaceutically acceptable carriers, excipients, emollients,stabilizers, etc., as are known in the pharmaceutical industry. In someembodiments, the term “consisting essentially of” refers to acomposition, whose only active ingredient is the indicated activeingredient, however, other compounds may be included which are forstabilizing, preserving, etc. the formulation, but are not involveddirectly in the therapeutic effect of the indicated active ingredient.In some embodiments, the term “consisting essentially of” may refer tocomponents, which exert a therapeutic effect via a mechanism distinctfrom that of the indicated active ingredient. In some embodiments, theterm “consisting essentially of” may refer to components, which exert atherapeutic effect and belong to a class of compounds distinct from thatof the indicated active ingredient. In some embodiments, the term“consisting essentially of” may refer to components, which exert atherapeutic effect and belong to a class of compounds distinct from thatof the indicated active ingredient, by acting via a different mechanismof action, for example, and representing an embodiment of thisinvention, polypeptides comprising T cell epitopes present in acomposition may be specifically combined with polypeptides comprising Bcell epitopes. In some embodiments, the term “consisting essentially of”may refer to components which facilitate the release of the activeingredient. In some embodiments, the term “consisting” refers to acomposition, which contains the active ingredient and a pharmaceuticallyacceptable carrier or excipient.

Further, as used herein, the term “comprising” is intended to mean thatthe system includes the recited elements, but not excluding others whichmay be optional. By the phrase “consisting essentially of” it is meant amethod that includes the recited elements but exclude other elementsthat may have an essential significant effect on the performance of themethod. “Consisting of” shall thus mean excluding more than traces ofother elements. Embodiments defined by each of these transition termsare within the scope of this invention.

In one embodiment, the present invention provides combined preparations.In one embodiment, the term “a combined preparation” defines especiallya “kit of parts” in the sense that the combination partners as definedabove can be dosed independently or by use of different fixedcombinations with distinguished amounts of the combination partnersi.e., simultaneously, concurrently, separately or sequentially. In someembodiments, the parts of the kit of parts can then, e.g., beadministered simultaneously or chronologically staggered, that is atdifferent time points and with equal or different time intervals for anypart of the kit of parts. The ratio of the total amounts of thecombination partners, in some embodiments, can be administered in thecombined preparation. In one embodiment, the combined preparation can bevaried, e.g., in order to cope with the needs of a patient subpopulationto be treated or the needs of the single patient which different needscan be due to a particular disease, severity of a disease, age, sex, orbody weight as can be readily made by a person skilled in the art.

In one embodiment, the term “a” or “one” or “an” refers to at least one.In one embodiment the phrase “two or more” may be of any denomination,which will suit a particular purpose. In one embodiment, “about” maycomprise a deviance from the indicated term of +1%, or in someembodiments, −1%, or in some embodiments, ±2.5%, or in some embodiments,±5%, or in some embodiments, ±7.5%, or in some embodiments, ±10%, or insome embodiments, ±15%, or in some embodiments, ±20%, or in someembodiments, ±25%.

The following examples are presented in order to more fully illustratethe preferred embodiments of the invention. They should in no way beconstrued, however, as limiting the broad scope of the invention.

EXPERIMENTAL DETAILS SECTION

General Experimental Methods

Cell Growth Conditions

HCC 1937, HCC 1954, HCC 38, T47D-Kbluc, MDA-MB-453, and MDA-MB-231 weregrown in RPMI-1640 medium containing 2 mM L-glutamine supplemented with10% fetal bovine serum (FBS). Cells were maintained in a 5% CO₂/95% airhumidified atmosphere at 37° C.

Sulforhodamine B (SRB) Assay

The SRB Assay was used to determine cell number during cytotoxocityexperiments. The following protocol was used:

-   -   1. Cells were detached with 0.25% trypsin.    -   2. Experimental cultures were cultured in 96-well microtiter        plates (200 uL growth medium per well; 1,000-200,000 cells per        well).    -   3. Cultures were fixed with 50 uL 50% TCA (4° C.). (see cell        fixation protocol for details).    -   4. Fixed cells were stained with 50 uL 0.4% (wt/vol) SRB in 1%        acetic acid for 10 minutes.    -   5. SRB was removed and the cultures were quickly* rinsed 5 times        with 1% acetic acid to remove unbound dye.**    -   6. Cultures were air-dried overnight until there was no visible        moisture.    -   7. The cellular protein-bound SRB was dissolved with 200 uL        unbuffered Tris base (10 mM, pH 10.5) for 30 minutes on a        rocking platform shaker.    -   8. Absorbance was read at 540 nm * quickly performing rinsing        process was to prevent desorption of protein-bound SRB**        completely removed residual wash solution by sharply flicking        plates over sink.

Fixation of Cells Attached to the Plastic Substratum

The following protocol was used for fixing cells:

-   -   a. 50 uL of 50% TCA (4° C.) was gently layered on the top of        growth medium in each well to make a final TCA concentration of        10%.    -   b. Cultures were incubated at 4° C. for 1 hour.    -   c. Cultures were washed 5 times with tap water to remove TCA,        growth medium, low-molecular-weight metabolites, and serum        protein.    -   d. Plates were air-dried until there was no visible moisture.

Example 1 Effect of Formula IX on Growth in Different Breast CancersCell Lines Expressing Androgen Receptor Materials and Methods

MDA-MB-231 and HCC-38 triple negative breast cancer cells were used toanalyze growth effects of various compounds.

MDA-MB-231 and HCC-38 triple negative breast cancer cells were infectedwith 200 μL or 500 μL adenovirus containing LacZ (negative control) orAR, and were treated with various AR ligands (agonists: DHT and FormulaIX, and antagonist: bicalutamide) or a non-AR binder that isstructurally similar to Formula IX, R-enantiomer to of Formula IX. Cellswere treated in charcoal stripped FBS (FIGS. 1C, 1E, 1G and 1I; 2C, 2Eand 2G) or full serum (FIGS. 1D, 1F, 1H and 1J; 2D, 2F and 2H) for 3days, fixed and stained with sulforhodamine blue (SRB) to measure cellviability. IC₅₀ values were calculated

Results

Expression of AR in cells infected with AR or LacZ was evaluated usingWestern blotting (FIG. 1A and FIG. 2A).

Only the AR agonists, DHT and Formula IX, inhibited MDA-MB-231 andHCC-38 triple negative breast cancer cell growth (FIGS. 1C, 1D, 1E, 1Fand FIGS. 2C, 2D, 2E and 2F). This inhibition was observed only in thepresence of AR (compare w/lacZ and w/AR). IC₅₀ values in AR positivecells for DHT and Formula IX are presented in FIG. 1B and FIG. 2B.

Example 2 Reversal of Effect of Formula IX on Growth Materials andMethods

To determine if the growth inhibition observed with DHT and Formula IXin AR positive cells is AR dependent, MDA-MB-231 cells were infectedwith adenovirus containing LacZ (negative control) or AR and weretreated with AR agonists, DHT or Formula IX, in the presence or absenceof the AR antagonist, bicalutamide. Cells were treated in charcoalstripped FBS (FIGS. 3A and 3C) or full serum (FIGS. 3B and 3D) for 3days, fixed and stained with sulforhodamine blue (SRB) to measure cellviability. IC₅₀ values were calculated.

Results

Both DHT and Formula IX required AR to inhibit MDA-MB-231 cell growth,as demonstrated by the weakened growth inhibitory effects in thepresence of bicalutamide (FIG. 3A, 3B, 3C, 3D). IC₅₀ values for DHT andFormula IX in AR positive cells pretreated with or without bicalutamideare presented in FIG. 3E.

Example 3 Effect of Ar Ligands on Breast Cancer Cell Growth Materialsand Methods

To determine if all AR ligands inhibit the growth of triple negativebreast cancer cells, MDA-MB-231 cells were infected with adenoviruscontaining LacZ or AR and were treated with various AR ligands(agonists: DHT, Formula VIII, Formula IX, Formula X, Formula XIII,Formula XIV; antagonist: bicalutamide) and a non-AR-binder: R-enantiomerof Formula IX. Cells were treated in charcoal stripped FBS (FIGS. 4A,4C, 4E, 4G, 4I, 4K, 4M and 4O) or full serum (4B, 4D, 4F, 4H, 4J, 4L, 4Nand 4P) for 3 days, fixed and stained with sulforhodamine blue (SRB) tomeasure cell viability. Anti-proliferative IC₅₀ values were calculatedin breast cancer cells and compared to transactivation values, i.e.,EC₅₀ (agonists) and IC₅₀ (antagonists) values, generated in HEK-293cells. The growth regulatory properties in breast cancer cells of thesemolecules in breast cancer cells are comparable to the transactivationvalues obtained in HEK-293 cells.

Results

Only AR agonists inhibited the growth of MDA-MB-231 cells (FIGS. 4A-4B,4E-4H, and 4K-4P) and the growth inhibitory potential of these ligandsrank order with their agonistic activity observed in HEK-293 cells (FIG.4Q).

Example 14 demonstrates as well that AR agonists inhibited theproliferation of MDA-MB-231 cells stably transfected with AR.

Example 4 AR Transactivation Assays in Breast Cancer Cells Materials andMethods

To ensure that the ligands that elicited growth inhibitory propertiesare agonists in MDA-MB-231 cells, AR transactivation assays wereperformed in MDA-MB-231 cells. Though AR transactivation assay wasperformed in HEK-293 cells, the ability of ligands to function asagonists or antagonists depends on cellular microenvironment. Hence,MDA-MB-231 cells were transfected using lipofectamine with AR, GRE-LUCto and CMV-LUC as normalization control. The cells were treated 24 hafter transfection and luciferase assay performed 48 h aftertransfection.

Results

FIG. 5 shows that all AR ligands that elicited anti-proliferativeactivity are agonists in MDA-MB-231 cells transfected with AR and theiragonist and growth inhibitory properties compare well. In other words,growth inhibitory ligands are AR agonists in MDA-MB-231 cellstransfected with AR.

Example 5 Analysis of Growth Inhibitory Effects in Breast Cancer CellsExpressing Estrogen Receptor Materials and Methods

To ensure that growth inhibitory effects in MDA-MB-231 cells areselective to AR, and to determine if the liganddependent-growth-inhibitory effects are exclusive to AR and also toensure that the effects are not artifacts of adenoviral infection,MDA-MB-231 triple negative breast cancer cells were infected with ER-αor ER-β adenovirus constructs and were treated with ER agonist:estradiol (E2) or ER antagonist: ICI-182,780 (ICI) in charcoal strippedserum (FIG. 6C) or full serum (FIGS. 6D and 6E) for 3 days. Cells werefixed and stained with sulforhodamine blue (SRB) to measure cellviability. Expression of ER in infected cells was evaluated usingWestern blotting.

Results

FIGS. 6A-6B show the presence or absence of ERα or ERβ in MDA-MB-231cells following transfection.

FIGS. 6C-6E show that over-expression of ER-α or ER-β in MDA-MB-231cells failed to promote growth inhibition either in the presence of ERagonists or antagonists. Thus, the observed growth inhibitory effects inMDA-MB-231 cells are selective to the presence of the AR and ARagonists.

Example 6 Effect of Ar Agonist on Morphology of Breast Cancer CellsMaterials and Methods

-   MDA-MB-231 cells were stably transfected with AR using lentivirus.    Following transfection, cells were treated for 3 days with the    indicated concentrations of DHT or bicalutamide. Live cells were    visualized using a light-microscope and photographed. The cells were    imaged at the same magnification and under the same microscopic    conditions.

Results

FIG. 7 shows that DHT altered the morphology of MDA-MB-231 cells intomore anchorage dependent and differentiated cells, indicating thatagonist-bound AR expressing breast cancer cells will have less invasiveand migratory properties (e.g., less likely to metastasize).

DHT and SARMs alter the morphology of AR-positive MDA-MB-231 cells.MDA-MB-231 cells were stably transfected with AR using lentivirus andwere treated with vehicle or AR agonists at the indicatedconcentrations. At the end of 3 days of incubation, the cells wereimaged under a microscope (40×).

DHT and SARMs, but not the AR antagonist, bicalutamide (data not shown),or the inactive isomer of formula IX, altered the morphology of thecells into a more anchorage-dependent phenotype. (FIG. 12).

Example 7 Cross-Reactivity of Formula VIII with Other Nuclear HormoneReceptors

In order to determine whether compounds of this invention affected othernuclear hormone receptor signaling, the ability of a compoundrepresented by formula VIII to stimulate (agonist) or inhibit(antagonist) ERα-, ERβ-, GR-, PR-, or MR-mediated transcriptionalactivation, was analyzed.

Materials and Methods

Transient Transfection

Rat GR, MR, PR, ER-α and ER-β were individually cloned into a pCR3.1vector backbone. Sequencing was performed to verify the absence of anymutations. HEK-293 cells were plated at 90,000 cells per well of a 24well plate in Dulbecco's Minimal Essential Media supplemented with 5%charcoal-stripped FBS. The cells were transfected using Lipofectamine(Invitrogen, Carlsbad, Calif.) with 0.25 μg GRE-LUC for GR, MR and PRand ERE-LUC for ER-α and ER-β, 0.5 ng CMV-LUC (renilla luciferase) and12.5-25 ng of the respective expression vector for each receptor. Thecells were treated 24 h after transfection with formula VIII in theabsence (agonist mode) and presence (antagonist mode) of known agonists(estradiol for ER; dexamethasone for GR; aldosterone for MR;progesterone for PR) as controls. Luciferase assays were performed 48 hafter transfection. Transcriptional activation values are represented asfirefly luciferase normalized to renilla luciferase.

Results

The agonist effects of formula VIII on ER-β, ER-α, GR, PR and MR weretested and compared to the activities of the known ligands, as well(FIG. 8). A compound of formula VIII failed to activate ER-β or ER-αeven at the highest tested concentration (1 μM) whereas 1 nM estradiolinduced ERα- and ERβ-mediated transactivation by 3- and 5-fold,respectively. A compound of formula VIII failed to activate GR- orMR-mediated transactivation. A compound of formula VIII at all thetested concentrations did not induce GR- or MR-mediated transactivation,whereas the known ligands (dexamethasone and aldosterone) induced theactivities of GR or MR by 70- and 60-fold, respectively, at aconcentration of 1 nM. However, a compound of formula VIII increased thetransactivation of PR at 1 μM and 10 μM by 3 and 8 fold, respectively.Progesterone activated PR by 23 fold at a 1 nM concentration, indicatingthat a compound of formula VIII is greater than 10.000-fold weaker thanthe endogenous agonist for PR.

The ability of a compound of formula VIII to inhibit the effects of aknown agonist for each of the above mentioned receptors was tested aswell.

Co-incubation of HEK 293 cells with the indicated concentrations offormula VIII failed to alter the estradiol-induced ER-β or ER-αactivity, dexamethasone-induced GR-mediated transactivation oraldosterone-induced MR-mediated transactivation.

A dose response curve for a compound of formula VIII in antagonist modepotently partially inhibited PR activity (FIG. 9). In comparison toformula IX, formula VIII is was 10-times more potent, and 100-times morepotent than R-enantiomer of formula IX. In comparison to RU486, formulaVIII was about 1,000 fold weaker as a PR antagonist, than RU486.

Compounds of formula VIII and IX are specific for the AR and do notstimulate or inhibit receptor-mediated transactivation of ERα, ERβ, GR,or MR. Unexpectedly, formula VIII exhibited moderate potency partialagonist activity for PR, and potent PR partial antagonism (see FIG. 9).Combined AR-agonism and PR-antagonism will be beneficial in certainbreast cancers (e.g., PR-positive breast cancers).

Example 8 Formula VIII Inhibits Triple Negative Breast Cancer Cell TumorGrowth in Mice Materials and Methods

-   MDA-MB-231-AR triple negative breast cancer cells (2 million    cells/mouse; MDA-MB-231 cells stably transfected with AR using    lentivirus) were mixed with matrigel (1:1) and injected    subcutaneously into the flanks of intact female nude mice    (n=5/group). When the tumors reached 150-200 mm³, the animals were    separated into two groups, one receiving vehicle and the other    receiving 30 mg/kg formula VIII orally. Tumor volume was measured    thrice weekly and % tumor growth inhibition (TGI) was calculated. At    the end of 35 days of treatment, the animals were sacrificed, tumors    excised, weighed, and collected for various analyses. Blood was    collected and serum separated for drug concentration measurement.

Results

Formula VIII significantly reduced the tumor growth with TGI of ˜75%(FIG. 10B). Tumor weights were also reduced by more than 50% by FormulaVIII treatment (FIG. 11C) as were tumor size (FIGS. 11A-B). Formula VIIIelicited these to results without any associated toxicity or changes inbody weight (FIG. 10A). Uterus weight also increased in response toformula VIII treatment (not shown), indicative of in vivo androgenicresponse.

In summary, the formula VIII SARM is extremely effective in regressingthe growth of AR expressing triple negative breast cancer xenografts inmice, and is likely to be effective in a wide variety of AR-positivebreast cancers in humans, as described supra and infra.

Example 9 Effect of Formula IX in Women with Metastatic or Er and/or ARPositive Refractory Breast Cancer

This clinical trial will assess the safety and efficacy of a compoundrepresented by the structure of Formula IX (Formula IX) in human femalesubjects who have estrogen receptor (ER) and androgen receptor (AR)positive metastatic breast cancer, and who have responded previously tohormone therapy. The goal of this study is to determine the importanceof the AR status as a therapeutic target in women with ER positivemetastatic breast cancer that have previously responded to hormonetherapy.

Materials and Methods

Subject Population

Female subjects with ER positive metastatic breast cancer who havepreviously been treated with up to 3 prior hormonal therapies for thetreatment of breast cancer. Subjects must have been treated with andresponded to previous adjuvant therapy for ≧3 years or hormonal therapyfor metastatic disease for ≧6 months prior to progression. Details ofsubject selection criteria are presented below:

To be eligible for participation in this study, subjects must meet allof the following criteria, including give voluntary, signed informedconsent in accordance with institutional policies; be a woman that hasbeen diagnosed with ER positive metastatic breast cancer; and beclinically confirmed as postmenopausal. Subjects must have undergone theonset of spontaneous, medical or surgical menopause prior to the startof this study. (Spontaneous menopause is defined as the naturalcessation of ovarian function as indicated by being amenorrheic for atleast 12 months. If the subject has been amenorrheic for ≧6 monthsbut<12 months they must have a serum FSH concentration of ≧50 mIU/mL andan estradiol concentration of ≦25 pg/mL; medical menopause is defined astreatment with a luteinizing hormone receptor hormone agonist; andsurgical menopause is defined as bilateral oophorectomy).

Additional requirement that subjects must meet include that they havebeen treated and responded to previous adjuvant hormonal therapy for ≧3years or previous hormonal therapy for metastatic disease for ≧6 monthsprior to disease progression; that they have not had radiation therapyfor breast cancer within 2 weeks of randomization in this study and arenot planned to have radiation therapy during participation in thisstudy. Subjects must be willing to provide tissue sample from a biopsyof a metastatic tumor lesion(s) for determination of AR and ER status.Tissue samples from a biopsy of a primary tumor lesion will also beprovided if available. Further subjects must have ECOG score≦2 and beage≧18 years.

Subjects with any of the following exclusion criteria will NOT beeligible for enrollment in this study: have triple negative breastcancer; have, in the judgment of the Investigator, a clinicallysignificant concurrent illness or psychological, familial, sociological,geographical or other concomitant condition that would not permitadequate follow-up and compliance with the study protocol; haveuncontrolled hypertension, congestive heart failure or angina; haveStage 4 chronic obstructive pulmonary disease (COPD); have positivescreen for Hepatitis B consisting of HBsAg (Hepatitis B SurfaceAntigen), unless subject was diagnosed>10 years prior to enrollment andno evidence of active liver disease; have ALT/SGOT or AST/SGPT above 1.5times the upper limit of normal (ULN); have positive screen forhepatitis A antibody IgM or HIV; have received chemotherapy formetastatic breast cancer within the 3 months prior to enrollment in thestudy or be expected to receive chemotherapy for metastatic breastcancer during the study; be currently taking testosterone,methyltestosterone, oxandrolone (Oxandrin®), oxymetholone, danazol,fluoxymesterone (Halotestin®), testosterone-like agents (such asdehydroepiandrosterone (DHEA), androstenedione, and other androgeniccompounds, including herbals), or antiandrogens; previous therapy withtestosterone and testosterone-like agents is acceptable with a 30-daywashout (if previous testosterone therapy was long term depot within thepast 6 months, the site should contact the medical monitor for thisstudy to determine appropriate washout period); have untreated oruncontrolled brain metastasis; have been diagnosed with or treated forcancer within the previous two years, other than breast cancer ornon-melanoma carcinoma of the skin

Androgen receptor (AR) status will be assessed in all subjects fromprimary and/or metastatic lesions after enrollment. It is expected thatthe majority (70-95%) of subjects with ER positive breast cancer alsowill express AR and prostate specific antigen (PSA) in their primarytumor samples (Niemeier L A, et. al. Androgen receptor in breast cancer:expression in estrogen receptor-positive tumors and in estrogen-negativetumors with apocrine differentiation. Modern Pathology 23:205-212, 2010;Narita D, et al. Immunohistochemical expression of androgen receptor andprostate-specific antigen in breast cancer. Folia Histochemica EtCytobiologica 44:165-172, 2006). High percentages (72-84%) of metastaticlesions obtained from women with advanced breast cancer have also beenfound to be AR positive (Lea O A. et al. Improved measurement ofandrogen receptors in human breast cancer. Cancer Research 49:7162-7167,1989).

As 70% or greater of the women with ER positive breast cancer areexpected to have tumors that are AR positive, the study is designed toenroll approximately 27 subjects with AR positive breast cancer in eachdose arm, enabling assessment of the primary endpoint in AR positivesubjects, as well as the secondary and tertiary endpoints in subsetsbased on AR status (i.e., all subjects, AR positive subjects, and ARnegative subjects).

Treatment

Subjects will receive either a 3 mg daily dose or 9 mg daily dose ofFormula IX in a staggered dose design, with baseline and regular onstudy assessments of safety and efficacy.

Forty (40) subjects will receive Formula IX 3 mg and 40 subjects willreceive Formula IX 9 mg. Enrollment into this study will be staggeredsuch that the first 40 subjects will be enrolled into the 3 mg FormulaIX dose arm. These subjects will be evaluated for efficacy and safety.When the last subject in the 3 mg Formula IX dose arm has been enrolledin this dose arm and there is acceptable safety based on a review ofadverse events and clinical benefit by the sponsor, enrollment for theremaining 40 subjects will commence in the 9 mg Formula IX dose arm.

TABLE 1 Dose Arm Dose N Capsules Administered Dose Arm 1 3 mg QD 40 1 ×3 mg soft gel capsule Dose Arm 2 9 mg QD 40 3 × 3 mg soft gel capsule

Measurable and non-measurable lesions (primary and/or metastatic) willbe identified and assessed by a modified Response Evaluation Criteria InSolid Tumors (RECIST 1.1) classification over the course of this study(described in detail below).

Study Duration

Each subject enrolled into this study will receive study interventionuntil a progression free survival (PFS) endpoint has been reached (tumorprogression or death). Subjects will be followed after treatment hasbeen discontinued for vital status only.

Efficacy Endpoints

The primary efficacy analysis will be the clinical benefit in subjectswith AR positive breast cancer at 6 months as measured by a modifiedResponse Evaluation Criteria In Solid Tumors (RECIST 1.1)classification. Key secondary endpoints of clinical benefit in allsubjects and AR negative subjects, as well as objective response rate,progression free survival, time to progression, duration of response,incidence of SREs, and time to first SRE in subsets based on AR status(i.e., all subjects, AR positive subjects, and AR negative subjects)will also be assessed. Effects on CA 27-29, PSA, bone turnover markers,QOL, and libido will be assessed as tertiary endpoints.

Primary Endpoint

Clinical benefit in a subject is defined as a complete response [CR], apartial response [PR] or stable disease [SD] as measured by modifiedRECIST 1.1, which is described in detail below. (Eisenhauer E A et al.New response evaluation criteria in solid tumors: revised RECISTguideline (version 1.1). European Journal of Cancer 45:228-247, 2009).

For subjects with non-measurable (non-target) disease only at baseline,SD will be defined as those with non-CR/non-PD combined response. Theprimary endpoint of the study will be to assess the proportion ofsubjects with clinical benefit (PCB) at 6 months (CR+PR+SD) in subjectswith AR positive breast cancer.

Secondary Endpoints

The secondary efficacy endpoints include:

To assess the clinical benefit in all subjects with breast cancertreated with Formula IX. The clinical benefit is defined as theproportion of subjects with complete response [CR]+partial response[PR]+stable disease [SD] as measured by modified RECIST 1.1 (EisenhauerE A et al. New response evaluation criteria in solid tumors: revisedRECIST guideline (Version 1.1). European Journal of Cancer 45:228-247,2009).

For subjects with non-measurable (non-target) disease only at baseline,SD will be defined as those with non-CR/non-PD combined response.

To assess objective response rate (ORR) in subjects with breast cancertreated with Formula IX. Objective response rate is defined as theproportion of subjects with a CR or PR at 6 months as measured bymodified RECIST 1.1. For subjects with non-measurable (non-target)disease only at baseline, ORR is defined as the proportion of subjectswith a CR at 6 months as measured by modified RECIST 1.1.

To assess progression free survival (PFS) in subjects with breast cancertreated with Formula IX. PFS is defined as the time elapsed betweentreatment initiation and tumor progression as measured by modifiedRECIST 1.1 OR death.

To assess time to progression (TTP) in subjects with breast cancertreated with Formula IX. Time to tumor progression is defined as thetime elapsed between treatment initiation and tumor progression asmeasured by modified RECIST 1.1.

To assess duration of response in subjects with breast cancer treatedwith Formula IX.

To assess incidence of skeletal related events (SREs) in subjectstreated with Formula IX.

To assess time to first skeletal related event (SRE) in subjects treatedwith Formula IX.

Tertiary Endpoints

To assess serum CA 27-29 changes in subjects with breast cancer treatedwith Formula IX.

To assess serum PSA changes in subjects with breast cancer treated withFormula IX

To assess changes in bone turnover markers (serum osteocalcin, serumcollagen type I cross linked C-telopeptide [CTX], serum collagen type Icross linked N-telopeptide [NTX], serum bone specific alkalinephosphatase, and urinary NTX in subjects treated with Formula IX.

To assess the effect of Formula IX on quality of life (QOL) as measuredby FACIT-F questionnaire in subjects treated with Formula IX.

To assess the effect of Formula IX on libido as measured by femalesexual function index (FSFI) questionnaire in subjects treated withFormula IX.

To explore the relationship of various levels of AR expression asdetermined by immunohistochemistry with primary, secondary and tertiaryobjectives

Modified RECIST 1.1

The modified RECIST 1.1 definitions described below will be applied:

Measurable Lesions

A measurable lesion is defined as one lesion whose longest diameter (LD)can be accurately measured as ≧10 mm CT or MRI technique by using a 5 mmcontiguous reconstruction algorithm.

Measurable lesions must be at least 2 times the slice thickness or atleast two times the size of the CT scan interval cut.

Lesions seen on chest x-ray but not confirmed by CT or MRI scan are notacceptable as measurable lesions for this study.

To be considered pathologically enlarged and measurable, a lymph nodemust be >15 mm in short axis when assessed by CT scan (CT scan slicethickness recommended to be no greater than 5 mm) At baseline and infollow-up, only the short axis will be measured and followed.

Measurable disease is defined as the presence of at least one measurablelesion.

All measurements will be taken and recorded in millimeters using anelectronic measurement method.

Non-Measurable Lesions

Non-measurable lesions are defined as any lesion(s) that are smallerthan the criteria for measurable lesions stated above (non-nodal lesionswith longest diameter<10 mm or pathological lymph nodes with ≧10 mm to<15 mm in short axis) or truly non measurable lesions (or sites ofdisease). Lesions considered to be truly non-measurable are bone lesions(lytic lesions or mixed lytic-blastic lesions without identifiable softtissue components, and blastic lesions), leptomeningeal disease,ascites, pleural/pericardial effusions, lymphangitis cutis/pulmonis,inflammatory breast disease, abdominal masses not confirmed by imagingtechniques, and cystic lesions.

Target Lesions

Target lesions must be measurable lesions.

All target lesions up to a maximum of two lesions per organ and fivelesions in total, representative of all involved organs, will beselected/confirmed as target lesions, recorded and measured at baseline.

Target lesions should be selected on the basis of their size (lesionswith the longest diameter) and their suitability for accurate repetitivemeasurements by CT/MRI imaging techniques and be most representative ofthe subject's tumor burden.

Target lesions will be measured in one dimension by the size estimationof their diameter. A sum of the diameters (longest for non-nodal lesionsand shortest for nodal lesions) for all target lesions will becalculated and reported for each time point.

The baseline sum of diameters will be used as reference to furthercharacterize the objective tumor response of the measurable dimension ofthe disease.

Non-Target Lesions

All other lesions (or sites of disease) and any measurable lesions thatwere not selected as target lesions) should be identified as non-targetlesions and indicated as present at baseline.

Measurements of the non-target lesions may be performed, however thecontinued presence or absence as well as the disappearance orprogression status of these lesions will be noted throughout follow-upassessments.

New Lesions

New lesions will be called at follow-up visits regardless of whetherthey occur in anatomic regions that were routinely subjected tofollow-up, or in regions without disease at baseline and for which afollow-up scan is performed for clinical suspicion of new disease. Newlymph nodes need to have a minimum size of 10 mm in their shortest axis.New non-nodal lesions need not to be measurable or to have a minimumsize. Measurements of new lesions may be performed.

Response Criteria Definitions

The following response criteria will be applied for target andnon-target lesions:

Target Lesion Response Criteria

Complete Response (CR): Disappearance of all target lesions. Targetlymph node lesions that become <10 mm in their shortest diameter will beconsidered to be normal (non-pathologic) and their actual measurementwill be recorded. Thus, it follows that if all target node lesions havebecome <10 mm, and all other non-nodal lesions have disappeared (whethertarget or non-target type), the overall response will be considered tobe a CR.

Partial Response (PR): At least a 30% decrease in the sum of diametersof target lesions, taking as reference the baseline sum of thediameters.

Stable Disease (SD): Neither sufficient shrinkage to qualify for PR norsufficient increase to qualify for PD taking as reference the smallestsum of diameters (nadir).

Progressive Disease (PD): At least a 20% increase in the sum of thediameters of target lesions taking as reference the smallest sum ofdiameters (nadir) recorded since the treatment started. In addition tothe relative increase of 20%, the sum of diameters must also demonstratean absolute increase of at least 5 mm

Not evaluable (NE): NE can be applied if repeated measurements cannot beassessed for reasons such as inadequate or missing imaging.

Non-Target Lesion Response Criteria

Complete Response (CR): Disappearance of all non-target lesions. Alllymph nodes must be non-pathological in size (<10 mm short axis).Disappearance of bone lesions identified on bone scintigraphy.

Non-CR/Non-PD: Persistence of one or more non-target lesions. Stability,decrease, or mild increase in uptake of bone lesions on bonescintigraphy.

Progressive Disease (PD): Unequivocal progression of existing non-targetlesions. A perceived increase in bone disease in a preexisting area willnot be considered progression. For bone scintigraphy, at least two newlesions are required to conclude to a definite presence of new lesionsunless one or more of these lesions are confirmed by radiography, CT orMRI.

Not Evaluable (NE): NE can be applied if repeated evaluations cannot beassessed for reasons such as inadequate or missing imaging.

Definitions of Combined Response at Each Time Point

Determination of an overall response for each time point is based on thecombination of responses for target, non-target, and the presence orabsence of new lesions using the algorithm outlined on tables C1 and C2below.

TABLE C1 Summary of Definitions of Response for Patients with Measurable(Target) Disease at Baseline Response of Combined Lesion Types CombinedTarget Lesions Non-Target Lesions New Lesions Response CR CR No CR CRNon-CR/non-PD or NE No PR PR CR, non-CR/non-PD, or NE No PR SD CR,non-CR/non-PD, or NE No SD PD Any Yes or No PD Any PD Yes or No PD AnyAny Yes PD NE Non-PD No NE Non-PD Non-PD NE NE

TABLE C2 Summary of Definitions of Response for Patients withNon-Measurable (Non-Target) Disease only at Baseline Response ofCombined Lesion Types Combined Non-Target Lesions New Lesions ResponseCR No CR Non-CR/non-PD No Non-CR/non-PD NE No NE PD Yes or No PD Any YesPD

Example 10 Synthesis of (S) Enantiomer of Formula VIII

(2R)-1-Methacryloylpyrrolidin-2-carboxylic Acid

D-Proline, 14.93 g, 0.13 mol) was dissolved in 71 mL of 2 N NaOH andcooled in an ice bath; the resulting alkaline solution was diluted withacetone (71 mL). An acetone solution (71 mL) of methacryloyl chloride(13.56 g, 0.13 mol) and 2 N NaOH solution (71 mL) were simultaneouslyadded over 40 min to the aqueous solution of D-proline in an ice bath.The pH of the mixture was kept at 10-11° C. during the addition of themethacryloyl chloride. After stirring (3 h, room temperature), themixture was evaporated in vacuo at a temperature at 35-45° C. to removeacetone. The resulting solution was washed with ethyl ether and wasacidified to pH 2 with concentrated HCl. The acidic mixture wassaturated with NaCl and was extracted with EtOAc (100 mL×3). Thecombined extracts were dried over Na₂SO₄, filtered through Celite, andevaporated in vacuo to give the crude product as a colorless oil.Recrystallization of the oil from ethyl ether and hexanes afforded 16.2g (68%) of the desired compound as colorless crystals: mp 102-103° C.;the NMR spectrum of this compound demonstrated the existence of tworotamers of the title compound. ¹H NMR (300 MHz, DMSO-d₆) δ 5.28 (s) and5.15 (s) for the first rotamer, 5.15 (s) and 5.03 (s) for the secondrotamer (totally 2H for both rotamers, vinyl CH₂), 4.48-4.44 for thefirst rotamer, 4.24-4.20 (m) for the second rotamer (totally 1H for bothrotamers, CH at the chiral canter), 3.57-3.38 (m, 2H, CH₂), 2.27-2.12(1H, CH), 1.97-1.72 (m, 6H, CH₂, CH, Me); ¹³C NMR (75 MHz, DMSO-d₆) δfor major rotamer 173.3, 169.1, 140.9, 116.4, 58.3, 48.7, 28.9, 24.7,19.5: for minor rotamer 174.0, 170.0, 141.6, 115.2, 60.3, 45.9, 31.0,22.3, 19.7; IR (KBr) 3437 (OH), 1737 (C═O), 1647 (CO, COOH), 1584, 1508,1459, 1369, 1348, 1178 cm¹; [α]_(D) ²⁶+80.8° (c=1, MeOH); Anal. Calcd.for C₉H₁₃NO₃: C, 59.00; H, 7.15; N, 7.65. Found: C, 59.13; H, 7.19; N,7.61.

(3R,8aR)-3-Bromomethyl-3-methyl-tetrahydro-pyrrolo[2,1-c][1,4]oxazine-1,4-dione

A solution of NBS (23.5 g, 0.132 mol) in 100 mL of DMF was addeddropwise to a stirred solution of the (methyl-acryloyl)-pyrrolidine(16.1 g, 88 mmol) in 70 mL of DMF under argon at room temperature, andthe resulting mixture was stirred 3 days. The solvent was removed invacuo, and a yellow solid was precipitated. The solid was suspended inwater, stirred overnight at room temperature, filtered, and dried togive 18.6 g (81%) (smaller weight when dried ˜34%) of the title compoundas a yellow solid: mp 152-154° C.; ¹H NMR (300 MHz, DMSO-d₆) δ 4.69 (dd,J=9.6 Hz, J=6.7 Hz, 1H, CH at the chiral center), 4.02 (d, J=11.4 Hz,1H, CHH_(a)), 3.86 (d, J=11.4 Hz, 1H, CHH_(b)), 3.53-3.24 (m, 4H, CH₂),2.30-2.20 (m, 1H, CH), 2.04-1.72 (m, 3H, CH₂ and CH), 1.56 (s, 2H, Me);¹³C NMR (75 MHz, DMSO-d₆) δ 167.3, 163.1, 83.9, 57.2, 45.4, 37.8, 29.0,22.9, 21.6; IR (KBr) 3474, 1745 (C═O), 1687 (C═O), 1448, 1377, 1360,1308, 1227, 1159, 1062 cm⁻¹; [α]_(D) ²⁶+124.5° (c=1.3, chloroform);Anal. Calcd. for C₉H₁₂BrNO₃: C, 41.24, H, 4.61, N, 5.34. Found: C,41.46; H, 4.64; N, 5.32.

(2R)-3-Bromo-2-hydroxy-2-methylpropanoic Acid

A mixture of bromolactone (18.5 g, 71 mmol) in 300 mL of 24% HBr washeated at reflux for 1 h. The resulting solution was diluted with brine(200 mL), and was extracted with ethyl acetate (100 mL×4). The combinedextracts were washed with saturated NaHCO₃ (100 mL×4). The aqueoussolution was acidified with concentrated HCl to pH=1, which, in turn,was extracted with ethyl acetate (100 mL×4). The combined organicsolution was dried over Na₂SO₄, filtered through Celite, and evaporatedin vacuo to dryness. Recrystallization from toluene afforded 10.2 g(86%) of the desired compound as colorless crystals: mp 107-109° C.; ¹HNMR (300 MHz, DMSO-d₆) δ 3.63 (d, J=10.1 Hz, 1H, CHH_(a)), 3.52 (d,J=10.1 Hz, 1H, CHH_(b)), 1.35 (s, 3H, Me); IR (KBr) 3434 (OH), 3300-2500(COOH), 1730 (C═O), 1449, 1421, 1380, 1292, 1193, 1085 cm⁻¹; [α]_(u)²⁶+10.5° (c=2.6, MeOH); Anal. Calcd. for C₄H₇BrO₃: C, 26.25, H, 3.86.Found: C, 26.28, H, 3.75.

Synthesis of(2R)-3-bromo-N-(3-chloro-4-cyanophenyl)-2-hydroxy-2-methylpropanamide

Thionyl chloride (7.8 g, 65.5 mmol) was added dropwise to a cooledsolution (less than 4° C.) of (R)-3-bromo-2-hydroxy-2-methylpropanoicacid (9.0 g, 49.2 mol) in 50 mL of THF under an argon atmosphere. Theresulting mixture was stirred for 3 h under the same condition. To thiswas added Et₃N (6.6 g, 65.5 mol) and stirred for 20 min under the samecondition. After 20 min, 4-amino-2-chlorobenzonitrile (5.0 g, 32.8 mmol)and 100 mL of THF were added and then the mixture was allowed to stirovernight at room temperature. The solvent was removed under reducedpressure to give a solid which was treated with 100 mL of H₂O, extractedwith EtOAc (2×150 mL). The combined organic extracts were washed withsaturated NaHCO₃ solution (2×100 mL) and brine (300 mL), successively.The organic layer was dried over MgSO₄ and concentrated under reducedpressure to give a solid which was purified from column chromatographyusing EtOAc/hexane (50:50) to give 7.7 g (49.4%) of target compound as abrown solid.

¹H NMR (CDCl₃/TMS) δ 1.7 (s, 3H, CH₃), 3.0 (s, 1H, OH), 3.7 (d, 1H, CH),4.0 (d, 1H, CH), 7.5 (d, 1H, ArH), 7.7 (d, 1H, ArH), 8.0 (s, 1H, ArH),8.8 (s, 1H, NH). MS: 342.1 (M+23). Mp 129° C.

Synthesis of(S)-N-(3-chloro-4-cyanophenyl)-3-(4-cyanophenoxy)-2-hydroxy-2-methylpropanamide

A mixture of bromoamide (2.0 g, 6.3 mmol), anhydrous K₂CO₃ (2.6 g, 18.9mmol) in 50 mL of acetone was heated to reflux for 2 h and thenconcentrated under reduced pressure to give a solid. The resulting solidwas treated with 4-cyanophenol (1.1 g, 9.5 mmol) and anhydrous K₂CO₃(1.7 g, 12.6 mmol) in 50 mL of 2-propanol was heated to reflux for 3 hand then concentrated under reduced pressure to give a solid. Theresidue was treated with 100 mL of H₂O and then extracted with EtOAc(2×100 mL). The combined EtOAc extracts were washed with 10% NaOH (4×100mL) and brine, successively. The organic layer was dried over MgSO₄ andthen concentrated under reduced pressure to give an oil which waspurified by column chromatography using EtOAc/hexane (50:50) to give asolid. The solid was recrystallized from CH₂Cl₂/hexane to give 1.4 g(61.6%) of(S)-N-(3-chloro-4-cyanophenyl)-3-(4-cyanophenoxy)-2-hydroxy-2-methylpropanamideas a colorless solid.

¹H NMR (CDCl₃/TMS) δ 1.61 (s, 3H, CH₃), 3.25 (s, 1H, OH), 4.06 (d,J=9.15 Hz, 1H, CH), 4.50 (d, J=9.15 Hz, 1H, CH), 6.97-6.99 (m, 2H, ArH),7.53-7.59 (m, 4H, ArH), 7.97 (d, J=2.01 Hz, 1H, ArH), 8.96 (s, 1H, NH).Calculated Mass: 355.1, [M+Na]⁺378.0. Mp: 103-105° C.

Example 11 Synthesis of (S) Enantiomer of Formula IX

Synthesis of(2R)-3-Bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide

Thionyl chloride (46.02 g, 0.39 mol) was added dropwise to a cooledsolution (less than 4° C.) of (R)-3-bromo-2-hydroxy-2-methylpropanoicacid (51.13 g, 0.28 mol) in 300 mL of THF under an argon atmosphere.(R)-3-bromo-2-hydroxy-2-methylpropanoic acid was prepared as describedin Example 10. The resulting mixture was stirred for 3 h under the samecondition. To this was added Et₃N (39.14 g, 0.39 mol) and stirred for 20min under the same condition. After 20 min,5-amino-2-cyanobenzotrifluoride (40.0 g, 0.21 mol), 400 mL of THF wereadded and then the mixture was allowed to stir overnight at roomtemperature. The solvent was removed under reduced pressure to give asolid which was treated with 300 mL of H₂O, extracted with EtOAc (2×400mL). The combined organic extracts were washed with saturated NaHCO₃solution (2×300 mL) and brine (300 mL). The organic layer was dried overMgSO₄ and concentrated under reduced pressure to give a solid which waspurified from column chromatography using CH₂Cl₂/EtOAc (80:20) to give asolid. This solid was recrystallized from CH₂Cl₂/hexane to give 55.8 g(73.9%) of(2R)-3-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamideas a light-yellow solid.

¹H NMR (CDCl₃/TMS) δ 1.66 (s, 3H, CH₃), 3.11 (s, 1H, OH), 3.63 (d,J=10.8 Hz, 1H, CH₂), 4.05 (d, J=10.8 Hz, 1H, CH₂), 7.85 (d, J=8.4 Hz,1H, ArH), 7.99 (dd, J=2.1, 8.4 Hz, 1H, ArH), 8.12 (d, J=2.1 Hz, 1H,ArH), 9.04 (bs, 1H, NH). Calculated Mass: 349.99, [M-H]⁻ 349.0. M.p.:124-126° C.

Synthesis of(S)-N-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(4-cyanophenoxy)-2-hydroxy-2-methylpropanamide

A mixture of bromoamide((2R)-3-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide,50 g, 0.14 mol), anhydrous K₂CO₃ (59.04 g, 0.43 mol), 4-cyanophenol(25.44 g, 0.21 mol) in 500 mL of 2-propanol was heated to reflux for 3 hand then concentrated under reduced pressure to give a solid. Theresulting residue was treated with 500 mL of H₂O and then extracted withEtOAc (2×300 mL). The combined EtOAc extracts were washed with 10% NaOH(4×200 mL) and brine. The organic layer was dried over MgSO₄ and thenconcentrated under reduced pressure to give an oil which was treatedwith 300 mL of ethanol and an activated carbon. The reaction mixture washeated to reflux for 1 h and then the hot mixture was filtered throughCelite. The filtrate was concentrated under reduced pressure to give anoil. This oil was purified by column chromatography using CH₂Cl₂/EtOAc(80:20) to give an oil which was crystallized from CH₂Cl₂/hexane to give33.2 g (59.9%) of(S)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-cyanophenoxy)-2-hydroxy-2-methylpropanamideas a colorless solid (a cotton type).

¹H NMR (CDCl₃/TMS) δ 1.63 (s, 3H, CH₃), 3.35 (s, 1H₂OH), 4.07 (d, J=9.04Hz, 1H, CH), 4.51 (d, J=9.04 Hz, 1H, CH), 6.97-6.99 (m, 2H, ArH),7.57-7.60 (m, 2H, ArH), 7.81 (d, J=8.55 Hz, 1H, ArH), 7.97 (dd, J=1.95,8.55 Hz, 1H, ArH), 8.12 (d, J=1.95 Hz, 1H, ArH), 9.13 (bs, 1H, NH).Calculated Mass: 389.10, [M-H]⁻ 388.1. Mp: 92-94° C.

Example 12 Synthesis of (R) Enantiomer of Formula IX

Synthesis of(2S)-3-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide(precursor to R-enantiomer of formula IX)

Thionyl chloride (46.02 g, 0.39 mol) was added dropwise to a cooledsolution (less than 4° C.) of (S)-3-bromo-2-hydroxy-2-methylpropanoicacid (51.13 g, 0.28 mol) in 300 mL of THF under an argon atmosphere. Theresulting mixture was stirred for 3 h under the same condition. To thiswas added Et₃N (39.14 g, 0.39 mol) and stirred for 20 min under the samecondition. After 20 min, 5-amino-2-cyanobenzotrifluoride (40.0 g, 0.21mol), 400 mL of THF were added and then the mixture was allowed to stirovernight at room temperature. The solvent was removed under reducedpressure to give a solid which was treated with 300 mL of H₂O, extractedwith EtOAc (2×400 mL). The combined organic extracts were washed withsaturated NaHCO₃ solution (2×300 mL) and brine (300 mL). The organiclayer was dried over MgSO₄ and concentrated under reduced pressure togive a solid which was purified from column chromatography usingCH₂Cl₂/EtOAc (80:20) to give a solid. This solid was recrystallized fromEtOAc/hexane to give 55.8 g (73.9%) of target compound as a light-yellowsolid.

¹H NMR (CDCl₃/TMS) δ 1.66 (s, 3H, CH₃), 3.11 (s, 1H, OH), 3.63 (d,J=10.8 Hz, 1H, CH₂), 4.05 (d, J=10.8 Hz, 1H, CH₂), 7.85 (d, J=8.4 Hz,1H, ArH), 7.99 (dd, J=2.1, 8.4 Hz, 1H, ArH), 8.12 (d, J=2.1 Hz, 1H,ArH), 9.04 (bs, 1H, NH).

Calculated Mass: 349.99, [M-H]⁻ 349.0. Mp: 124-126° C.

Synthesis of(R)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-cyanophenoxy)-2-hydroxy-2-methylpropanamide(R-enantiomer of formula IX)

A mixture of bromoamide (50.0 g, 0.14 mol), anhydrous K₂CO₃ (59.04 g,0.43 mol), 4-cyanophenol (25.44 g, 0.21 mol) in 500 mL of 2-propanol washeated to reflux for 3 h and then concentrated under reduced pressure togive a solid. The resulting residue was treated with 500 mL of H₂O andthen extracted with EtOAc (2×300 mL). The combined EtOAc extracts werewashed with 10% NaOH (4×200 mL) and brine. The organic layer was driedover MgSO₄ and then concentrated under reduced pressure to give an oilwhich was treated with 300 mL of ethanol and an activated carbon. Thereaction mixture was heated to reflux for 1 h and then the hot mixturewas filtered through Celite. The filtrate was concentrated under reducedpressure to give an oil. This oil was purified by column chromatographyusing hexane/EtOAc (20:80) to give an oil which was crystallized fromEtOAc/hexane to give 33.2 g (59.9%) of(R)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-cyanophenoxy)-2-hydroxy-2-methylpropanamide(R-isomer of formula IX) as a colorless solid.

¹H NMR (CDCl₃/TMS) δ 1.63 (s, 3H, CH₃), 3.44 (s, 1H₂OH), 4.07 (d, J=9.16Hz, 1H, CH), 4.51 (d, J=9.16 Hz, 1H, CH), 6.97-6.99 (m, 2H, ArH),7.57-7.59 (m, 2H, ArH), 7.81 (d, J=8.54 Hz, 1H, ArH), 7.97 (dd, J=2.07,8.54 Hz, 1H, ArH), 8.12 (d, J=2.07 Hz, 1H, ArH), 9.15 (bs, 1H, NH).Calculated Mass: 389.10, [M-H]⁻ 388.1. Mp: 92-94° C.

Example 13 Synthesis of (S) Enantiomer of Formula X

Synthesis of(2R)-3-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide

Thionyl chloride (46.02 g, 0.39 mol) was added dropwise to a cooledsolution (less than 4° C.) of R-131 (51.13 g, 0.28 mol) in 300 mL of THFunder an argon atmosphere. The resulting mixture was stirred for 3 hunder the same condition. To this was added Et₃N (39.14 g, 0.39 mol) andstirred for 20 min under the same condition. After 20 min,5-amino-2-cyanobenzotrifluoride (40.0 g, 0.21 mol), 400 mL of THF wereadded and then the mixture was allowed to stir overnight at roomtemperature. The solvent was removed under reduced pressure to give asolid which was treated with 300 mL of H₂O, extracted with EtOAc (2×400mL). The combined organic extracts were washed with saturated NaHCO₃solution (2×300 mL) and brine (300 mL). The organic layer was dried overMgSO₄ and concentrated under reduced pressure to give a solid which waspurified by column chromatography using CH₂Cl₂/EtOAc (80:20) to give asolid. This solid was recrystallized from CH₂Cl₂/hexane to give a targetcompound (55.8 g, 73.9%) as a light-yellow solid.

¹H NMR (CDCl₃/TMS) δ 1.66 (s, 3H, CH₃), 3.11 (s, 1H, OH), 3.63 (d,J=10.8 Hz, 1H, CH₂), 4.05 (d, J=10.8 Hz, 1H, CH₂), 7.85 (d, J=8.4 Hz,1H, ArH), 7.99 (dd, J=2.1, 8.4 Hz, 1H, ArH), 8.12 (d, J=2.1 Hz, 1H,ArH), 9.04 (bs, 1H, NH). Calculated Mass: 349.99, [M-H]⁻ 349.0. Mp:124-126° C.

Synthesis of(S)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-fluorophenoxy)-2-hydroxy-2-methylpropanamide(Formula X)

A mixture of bromoamide (10.0 g, 28.5 mmol), anhydrous K₂CO₃ (11.8 g,85.4 mmol) in 150 mL of acetone was heated to reflux for 1 h and thenconcentrated under reduced pressure to give a solid. The resultingresidue was treated with 4-fluorophenol (4.8 g, 42.7 mmol), anhydrousK₂CO₃ (7.9 g, 57.0 mmol), 150 mL of 2-propanol and then heated to refluxfor 2 h. The resulting mixture was concentrated under reduced pressureto give a solid. This solid was treated with 300 mL of H₂O and extractedwith EtOAc (2×250 mL). The combined EtOAc extracts were washed with asaturated NaHCO₃ solution (2×250 mL) and brine. The organic layer wasdried over MgSO₄ and then concentrated under reduced pressure to give anoil which was purified by column chromatography using CH₂Cl₂/EtOAc(80:20) to give a solid. This solid was recrystallized fromCH₂Cl₂/hexane to give(S)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-fluorophenoxy)-2-hydroxy-2-methylpropanamide(Formula X, 10.04 g, 92.2%) as a colorless solid.

¹H NMR (CDCl₃/TMS) δ 1.59 (s, 3H, CH₃), 3.36 (s, 1H₂OH), 3.95 (d, J=9.00Hz, 1H, CH), 4.43 (d, J=9.00 Hz, 1H, CH), 6.87-6.88 (m, 2H, ArH),6.96-7.02 (m, 2H, ArH), 7.81 (d, J=8.45 Hz, 1H, ArH), 7.94-7.98 (m, 1H,ArH), 8.10 (d, J=1.79 Hz, 1H, ArH), 9.11 (s, 1H, NH). Calculated Mass:382.31, [M-H]⁻ 380.9. Mp: 139-141° C.

Example 14 Synthesis of (S) Enantiomer of Formula XIII

Synthesis of(2R)-3-Bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide

Thionyl chloride (46.02 g, 0.39 mol) was added dropwise to a cooledsolution (less than 4° C.) of R-18 (51.13 g, 0.28 mol) in 300 mL of THFunder an argon atmosphere. R-18 is(R)-3-bromo-2-hydroxy-2-methylpropanoic acid was prepared as describedin Example 10. The resulting mixture was stirred for 3 h under the samecondition. To this was added Et₃N (39.14 g, 0.39 mol) and stirred for 20min under the same condition. After 20 min,5-amino-2-cyanobenzotrifluoride (40.0 g, 0.21 mol), 400 mL of THF wereadded and then the mixture was allowed to stir overnight at roomtemperature. The solvent was removed under reduced pressure to give asolid which was treated with 300 mL of H₂O, extracted with EtOAc (2×400mL). The combined organic extracts were washed with saturated NaHCO₃solution (2×300 mL) and brine (300 mL). The organic layer was dried overMgSO₄ and concentrated under reduced pressure to give a solid which waspurified from column chromatography using CH₂Cl₂/EtOAc (80:20) to give asolid. This solid was recrystallized from CH₂Cl₂/hexane to give 55.8 g(73.9%) of(2R)-3-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide(R-19) as a light-yellow solid.

¹H NMR (CDCl₃/TMS) δ 1.66 (s, 3H, CH₃), 3.11 (s, 1H, OH), 3.63 (d,J=10.8 Hz, 1H, CH₂), 4.05 (d, J=10.8 Hz, 1H, CH₂), 7.85 (d, J=8.4 Hz,1H, ArH), 7.99 (dd, J=2.1, 8.4 Hz, 1H, ArH), 8.12 (d, J=2.1 Hz, 1H,ArH), 9.04 (bs, 1H, NH). Calculated Mass: 349.99, [M-H]⁻ 349.0. M.p.:124-126° C.

Synthesis of(S)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-cyano-3-fluorophenoxy)-2-hydroxy-2-methylpropanamide(Formula XIII)

A mixture of bromoamide((2R)-3-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide,R-19 (2.0 g, 5.70 mmol), anhydrous K₂CO₃ (2.4 g, 17.1 mmol) in 50 mL ofacetone was heated to reflux for 2 h and then concentrated under reducedpressure to give a solid. The resulting solid was treated with2-fluoro-4-hydroxybenzonitrile (1.2 g, 8.5 mmol) and anhydrous K₂CO₃(1.6 g, 11.4 mmol) in 50 mL of 2-propanol was heated to reflux for 3 hand then concentrated under reduced pressure to give a solid. Theresidue was treated with 100 mL of H₂O and then extracted with EtOAc(2×100 mL). The combined EtOAc extracts were washed with 10% NaOH (4×100mL) and brine, successively. The organic layer was dried over MgSO₄ andthen concentrated under reduced pressure to give an oil which wascrystallized from CH₂Cl₂/hexane to give 0.5 g (23%) of(S)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-cyano-3-fluorophenoxy)-2-hydroxy-2-methylpropanamideas a colorless solid.

¹H NMR (CDCl₃/TMS) δ 1.63 (s, 3H, CH₃), 3.34 (bs, 1H₂OH), 4.08 (d,J=9.17 Hz, 1H, CH), 4.50 (d, J=9.17 Hz, 1H, CH), 6.74-6.82 (m, 2H, ArH),7.50-7.55 (m, 1H, ArH), 7.81 (d, J=8.50 Hz, 1H, ArH), 7.97 (q, J=2.03,8.50 Hz, 1H, ArH), 8.11 (d, J=2.03 Hz, 1H, ArH), 9.12 (s, 1H, NH).Calculated Mass: 407.1, 1M+Na]⁺ 430.0. Mp: 124-125° C.

Example 15 Synthesis of (S) Enantiomer of Formula XIV

Synthesis of(2R)-3-Bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide

Thionyl chloride (46.02 g, 0.39 mol) was added dropwise to a cooledsolution (less than 4° C.) of R-18 (51.13 g, 0.28 mol) in 300 mL of THFunder an argon atmosphere. R-18 is(R)-3-bromo-2-hydroxy-2-methylpropanoic acid was prepared as describedin Example 10. The resulting mixture was stirred for 3 h under the samecondition. To this was added Et₃N (39.14 g, 0.39 mol) and stirred for 20min under the same condition. After 20 min,5-amino-2-cyanobenzotrifluoride (40.0 g, 0.21 mol), 400 mL of THF wereadded and then the mixture was allowed to stir overnight at roomtemperature. The solvent was removed under reduced pressure to give asolid which was treated with 300 mL of H₂O, extracted with EtOAc (2×400mL). The combined organic extracts were washed with saturated NaHCO₃solution (2×300 mL) and brine (300 mL). The organic layer was dried overMgSO₄ and concentrated under reduced pressure to give a solid, which waspurified from column chromatography using CH₂Cl₂/EtOAc (80:20) to give asolid. This solid was recrystallized from CH₂Cl₂/hexane to give 55.8 g(73.9%) of(2R)-3-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide(R-19) as a light-yellow solid.

¹H NMR (CDCl₃/TMS) δ 1.66 (s, 3H, CH₃), 3.11 (s, 1H, OH), 3.63 (d,J=10.8 Hz, 1H, CH₂), 4.05 (d, J=10.8 Hz, 1H, CH₂), 7.85 (d, J=8.4 Hz,1H, ArH), 7.99 (dd, J=2.1, 8.4 Hz, 1H, ArH), 8.12 (d, J=2.1 Hz, 1H,ArH), 9.04 (bs, 1H, NH). Calculated Mass: 349.99, [M-H]⁻ 349.0. M.p.:124-126° C.

Synthesis of(S)-3-(4-chloro-3-fluorophenoxy)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide(Formula XIV)

A mixture of bromoamide((2R)-3-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide,(R-19) 2.0 g, 5.70 mmol), anhydrous K₂CO₃ (2.4 g, 17.1 mmol) was heatedto reflux for 2 h and then concentrated under reduced pressure to give asolid. The resulting solid was treated with 4-chloro-3-fluorophenol (1.3g, 8.5 mmol) and anhydrous K₂CO₃ (1.6 g, 11.4 mmol) in 50 mL of2-propanol was heated to reflux for 3 h and then concentrated underreduced pressure to give a solid. The residue was treated with 100 mL ofH₂O and then extracted with EtOAc (2×100 mL). The combined EtOAcextracts were washed with 10% NaOH (4×100 mL) and brine, successively.The organic layer was dried over MgSO₄ and then concentrated underreduced pressure to give an oil which was purified by columnchromatography using EtOAc/hexane (50:50) to give a solid which wasrecrystallized from CH₂Cl₂/hexane to give 1.7 g (70.5%) of(S)-3-(4-chloro-3-fluorophenoxy)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamideas a colorless solid.

¹H NMR (CDCl₃/TMS) δ 1.60 (s, 3H, CH₃), 3.28 (s, 1H, OH), 3.98 (d,J=9.05 Hz, 1H, CH), 6.64-6.76 (m, 2H, ArH), 7.30 (d, J=8.67 Hz, 1H,ArH), 7.81 (d, J=8.52 Hz, 1H, ArH), 7.96 (q, J=2.07, 8.52 Hz, 1H, ArH),8.10 (d, J=2.07 Hz, 1H, ArH), 9.10 (s, 1H, NH). Calculated Mass: [M-H]⁻414.9. Mp: 132-134° C.

Example 16 Binding and Transactivation of SARMS in Breast Cancer Cells

In order to determine whether compounds of this invention are agonistsin breast cancer cells, HEK-293 or MDA-MB-231 cells were transfectedwith 0.25 μg GRE-LUC, 10 ng CMV-renilla LUC, and 25 ng CMV-hAR usinglipofectamine. Twenty four hours after transfection, the cells weretreated with DHT, compound of formula VIII and compound of formula IXand luciferase assay performed 48 hrs after transfection. Competitivebinding of DHT, compound of formula VIII and compound of formula IX weremeasured using an in vitro competitive radioligand binding assay with[17α-methyl-3H]-Mibolerone ([3H]MIB), a known steroidal and highaffinity AR ligand, and purified AR-LBD protein.

Results

DHT, compound of formula VIII and formula IX are agonists of AR inbreast cancer cells as presented in FIG. 13. The relative bindingaffinities (RBAs) for AR of DHT, formula IX, formula VIII, andbicalutamide were 1.0, 0.330, 0.314, and 0.016, respectively,demonstrating high affinity AR binding for the SARM compounds of thisinvention.

Example 17 Inhibition of Intratumoral Gene Expression

AR agonists differentially regulate genes in AR-positive and AR-negativebreast cancer cells. MDA-MB-231 and MCF-7 cells infected with AR or GFPcontaining adenovirus were maintained in charcoal stripped serumcontaining medium for 3 days and were treated with DHT or Compound VIII.After overnight treatment, the cells were harvested, RNA isolated andreal-time PCR for the indicated genes were performed. The expression ofvarious genes in response to either DHT or Compound VIII were measuredand normalized to GAPDH, and are presented as composite data (sameeffects for DHT and Compound VIII) in Table 2.

TABLE 2 Differential Regulation of Gene Expression by AR Ligands inER-Positive (MCF7) and ER-Negative (MDA-MB-231) Breast Cancers AR PSAMuc1 SLUG VCAM1 SPARC MMP2 MDA-MB-231/ GFP — — — — — MDA-MB-231/AR

— ↓ ↓ ↓ MDA-MB-231/AR

— ↓ ↓ ↓ cs FBS MCF7/GFP — — no — no MCF7 /AR —

no — no MCF7 AR — ↑ no — no cs FBS VCAM1- Vascular cell adhesionprotein-1 - Important for anchorage-dependent growth of cells and alsois a chemoattractant. SPARC - Secreted protein acidic and rich incysteine (aka Osteonectin) - extracellular glycoprotein important forangiogenesis. MUC1 - Mucinl - Extracellular glycoprotein associated withcancers - Its promoter has a strong ARE. SLUG - Zinc fingertranscription factor - Its promoter has a strong ARE. MMP2 - matrixmetalloproteinase-2 - gene that is activated by cell-cell clustering.

While certain features of the invention have been illustrated anddescribed herein, many modifications, substitutions, changes, andequivalents will now occur to those of ordinary skill in the art. It is,therefore, to be understood that the appended claims are intended tocover all such modifications and changes as fall within the true spiritof the invention.

What is claimed is:
 1. A method of treating a subject suffering frombreast cancer, comprising the step of administering to said subject aselective androgen receptor modulator (SARM) compound represented by astructure of formula I:

X is a bond, O, CH₂, NH, S, Se, PR, NO or NR; G is O or S; T is OH, OR,—NHCOCH₃, or NHCOR; R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl,CH₂F, CHF₂, CF₃, CF₂CF₃, aryl, phenyl, halogen, alkenyl or OH; R₁ isCH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃; R₂ is H, F, Cl, Br, I, CH₃,CF₃, OH, CN, NO₂, NHCOCH₃, NHCOCF₃, NHCOR, alkyl, arylalkyl, OR, NH₂,NHR, N(R), SR; R₃ is H, F, Cl, Br, I, CN, NO₂, COR, COOH, CONHR, CF₃,Sn(R)₃, or R₃ together with the benzene ring to which it is attachedforms a fused ring system represented by the structure:

Z is NO₂, CN, COR, COOH, or CONHR; Y is CF₃, F, Br, Cl, I, CN, orSn(R)₃; Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃, NHCOR,NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃, NHSO₂R,OR, COR, OCOR, OSO₂R, SO₂R or SR; or Q together with the benzene ring towhich it is attached is a fused ring system represented by structure A,B or C:

n is an integer of 1-4; and m is an integer of 1-3.
 2. The method ofclaim 1, wherein said SARM compound is represented by a structure offormula XIII:

or formula XIV:


3. The method of claim 1, wherein said SARM compound is represented by astructure of formula II:

wherein X is a bond, O, CH₂, NH, Se, PR, or NR; G is O or S; T is OH,OR, —NHCOCH₃, or NHCOR; Z is NO₂, CN, COR, COOH or CONHR; Y is I, CF₃,Br, Cl, or Sn(R)₃; Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃,NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃,NHSO₂R, OR, COR, OCOR, OSO₂R, SO₂R or SR; or Q together with the benzenering to which it is attached is a fused ring system represented bystructure A, B or C:

R is a C₁-C₄ alkyl, aryl, phenyl, alkenyl, hydroxyl, a C₁-C₄ haloalkyl,halogen, or haloalkenyl; and R₁ is CH₃, CF₃, CH₂CH₃, or CF₂CF₃.
 4. Themethod of claim 3, wherein said SARM compound is represented by astructure of formula:

5-6. (canceled)
 7. The method of claim 1 or 3, wherein said breastcancer is a breast cancer that has failed selective estrogen receptormodulator SERM (tamoxifen, toremifene), aromatase inhibitor, trastuzumab(Herceptin, ado-trastuzumab emtansine), pertuzumab (Perjeta), lapatinib,exemestane (Aromasin), pertuzumab (Perjeta), exemestance (Aromasin),bevacizumab (Avastin), and/or fulvestrant treatments.
 8. A method oftreating a subject suffering from metastatic breast cancer, or advancedbreast cancer comprising the step of administering to said subject aselective androgen receptor modulator (SARM) compound represented by astructure of formula I:

X is a bond, O, CH₂, NH, S, Se, PR, NO or NR; G is O or S; T is OH, OR,—NHCOCH₃, or NHCOR; R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl,CH₂F, CHF₂, CF₃, CF₂CF₃, aryl, phenyl, halogen, alkenyl or OH; R₁ isCH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃; R₂ is H, F, Cl, Br, I, CH₃,CF₃, OH, CN, NO₂, NHCOCH₃, NHCOCF₃, NHCOR, alkyl, arylalkyl, OR, NH₂,NHR, N(R), SR; R₃ is H, F, Cl, Br, I, CN, NO₂, COR, COOH, CONHR, CF₃,Sn(R)₃, or R₃ together with the benzene ring to which it is attachedforms a fused ring system represented by the structure:

Z is NO₂, CN, COR, COOH, or CONHR; Y is CF₃, F, Br, Cl, I, CN, orSn(R)₃; Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃, NHCOR,NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃, NHSO₂R,OR, COR, OCOR, OSO₂R, SO₂R or SR; or Q together with the benzene ring towhich it is attached is a fused ring system represented by structure A,B or C:

n is an integer of 1-4; and m is an integer of 1-3.
 9. The method ofclaim 8, wherein said SARM compound is represented by a structure offormula XIII:

or formula XIV:


10. The method of claim 8, wherein said SARM compound is represented bya structure of formula II:

wherein X is a bond, O, CH₂, NH, Se, PR, or NR; G is O or S; T is OH,OR, —NHCOCH₃, or NHCOR; Z is NO₂, CN, COR, COOH or CONHR; Y is I, CF₃,Br, Cl, or Sn(R)₃; Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃,NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃,NHSO₂R, OR, COR, OCOR, OSO₂R, SO₂R or SR; or Q together with the benzenering to which it is attached is a fused ring system represented bystructure A, B or C:

R is a C₁-C₄ alkyl, aryl, phenyl, alkenyl, hydroxyl, a C₁-C₄ haloalkyl,halogen, or haloalkenyl; and R₁ is CH₃, CF₃, CH₂CH₃, or CF₂CF₃.
 11. Themethod of claim 10, wherein said SARM compound is represented by astructure of formula:

12-13. (canceled)
 14. The method of claim 8, wherein said metastaticbreast cancer is AR-positive metastatic breast cancer.
 15. A method oftreating a subject suffering from refractory breast cancer, comprisingthe step of administering to said subject a selective androgen receptormodulator (SARM) compound represented by a structure of formula I:

X is a bond, O, CH₂, NH, S, Se, PR, NO or NR; G is O or S; T is OH, OR,—NHCOCH₃, or NHCOR; R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl,CH₂F, CHF₂, CF₃, CF₂CF₃, aryl, phenyl, halogen, alkenyl or OH; R₁ isCH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃; R₂ is H, F, Cl, Br, I, CH₃,CF₃, OH, CN, NO₂, NHCOCH₃, NHCOCF₃, NHCOR, alkyl, arylalkyl, OR, NH₂,NHR, N(R), SR; R₃ is H, F, Cl, Br, I, CN, NO₂, COR, COOH, CONHR, CF₃,Sn(R)₃, or R₃ together with the benzene ring to which it is attachedforms a fused ring system represented by the structure:

Z is NO₂, CN, COR, COOH, or CONHR; Y is CF₃, F, Br, Cl, I, CN, orSn(R)₃; Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃, NHCOR,NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃, NHSO₂R,OR, COR, OCOR, OSO₂R, SO₂R or SR; or Q together with the benzene ring towhich it is attached is a fused ring system represented by structure A,B or C:

n is an integer of 1-4; and m is an integer of 1-3.
 16. The method ofclaim 15, wherein said SARM compound is represented by a structure offormula XIII:

or formula XIV:


17. The method of claim 15, wherein said SARM compound is represented bya structure of formula II:

wherein X is a bond, O, CH₂, NH, Se, PR, or NR; G is O or S; T is OH,OR, —NHCOCH₃, or NHCOR; Z is NO₂, CN, COR, COOH or CONHR; Y is I, CF₃,Br, Cl, or Sn(R)₃; Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃,NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃,NHSO₂R, OR, COR, OCOR, OSO₂R, SO₂R or SR; or Q together with the benzenering to which it is attached is a fused ring system represented bystructure A, B or C:

R is a C₁-C₄ alkyl, aryl, phenyl, alkenyl, hydroxyl, a C₁-C₄ haloalkyl,halogen, or haloalkenyl; and R₁ is CH₃, CF₃, CH₂CH₃, or CF₂CF₃.
 18. Themethod of claim 17, wherein said SARM compound is represented by astructure of formula:

19-20. (canceled)
 21. The method of claim 15, wherein said refractorybreast cancer is AR-positive refractory breast cancer.
 22. A method oftreating a subject suffering from AR-positive breast cancer, comprisingthe step of administering to said subject a selective androgen receptormodulator (SARM) compound represented by a structure of formula I:

X is a bond, O, CH₂, NH, S, Se, PR, NO or NR; G is O or S; T is OH, OR,—NHCOCH₃, or NHCOR; R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl,CH₂F, CHF₂, CF₃, CF₂CF₃, aryl, phenyl, halogen, alkenyl or OH; R₁ isCH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃; R₂ is H, F, Cl, Br, I, CH₃,CF₃, OH, CN, NO₂, NHCOCH₃, NHCOCF₃, NHCOR, alkyl, arylalkyl, OR, NH₂,NHR, N(R)₂, SR; R₃ is H, F, Cl, Br, I, CN, NO₂, COR, COOH, CONHR, CF₃,Sn(R)₃, or R₃ together with the benzene ring to which it is attachedforms a fused ring system represented by the structure:

Z is NO₂, CN, COR, COOH, or CONHR; Y is CF₃, F, Br, Cl, I, CN, orSn(R)₃; Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃, NHCOR,NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃, NHSO₂R,OR, COR, OCOR, OSO₂R, SO₂R or SR; or Q together with the benzene ring towhich it is attached is a fused ring system represented by structure A,B or C:

n is an integer of 1-4; and m is an integer of 1-3.
 23. The method ofclaim 22, wherein said SARM compound is represented by a structure offormula XIII:

or formula XIV:


24. The method of claim 22, wherein said SARM compound is represented bya structure of formula II:

wherein X is a bond, O, CH₂, NH, Se, PR, or NR; G is O or S; T is OH,OR, —NHCOCH₃, or NHCOR; Z is NO₂, CN, COR, COOH or CONHR; Y is I, CF₃,Br, Cl, or Sn(R)₃; Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃,NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃,NHSO₂R, OR, COR, OCOR, OSO₂R, SO₂R or SR; or Q together with the benzenering to which it is attached is a fused ring system represented bystructure A, B or C:

R is a C₁-C₄ alkyl, aryl, phenyl, alkenyl, hydroxyl, a C₁-C₄ haloalkyl,halogen, or haloalkenyl; and R₁ is CH₃, CF₃, CH₂CH₃, or CF₂CF₃.
 25. Themethod of claim 24, wherein said SARM compound is represented by astructure of formula:

26-27. (canceled)
 28. The method of claim 22, wherein said AR-positivebreast cancer is AR-positive refractory breast cancer.
 29. The method ofclaim 22, wherein said AR-positive breast cancer is AR-positivemetastatic breast cancer.
 30. A method of treating a subject sufferingfrom triple negative breast cancer, comprising the step of administeringto said subject a selective androgen receptor modulator (SARM) compoundrepresented by a structure of formula I:

X is a bond, O, CH₂, NH, S, Se, PR, NO or NR; G is O or S; T is OH, OR,—NHCOCH₃, or NHCOR; R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl,CH₂F, CHF₂, CF₃, CF₂CF₃, aryl, phenyl, halogen, alkenyl or OH; R₁ isCH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃; R₂ is H, F, Cl, Br, I, CH₃,CF₃, OH, CN, NO₂, NHCOCH₃, NHCOCF₃, NHCOR, alkyl, arylalkyl, OR, NH₂,NHR, N(R)₂, SR; R₃ is H, F, Cl, Br, I, CN, NO₂, COR, COOH, CONHR, CF₃,Sn(R)₃, or R₃ together with the benzene ring to which it is attachedforms a fused ring system represented by the structure:

Z is NO₂, CN, COR, COOH, or CONHR; Y is CF₃, F, Br, Cl, I, CN, orSn(R)₃; Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃, NHCOR,NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃, NHSO₂R,OR, COR, OCOR, OSO₂R, SO₂R or SR; or Q together with the benzene ring towhich it is attached is a fused ring system represented by structure A,B or C:

n is an integer of 1-4; and m is an integer of 1-3.
 31. The method ofclaim 30, wherein said SARM compound is represented by a structure offormula XIII:

or formula XIV:


32. The method of claim 30, wherein said SARM compound is represented bya structure of formula II:

wherein X is a bond, O, CH₂, NH, Se, PR, or NR; G is O or S; T is OH,OR, —NHCOCH₃, or NHCOR; Z is NO₂, CN, COR, COOH or CONHR; Y is I, CF₃,Br, Cl, or Sn(R)₃; Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃,NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃,NHSO₂R, OR, COR, OCOR, OSO₂R, SO₂R or SR; or Q together with the benzenering to which it is attached is a fused ring system represented bystructure A, B or C:

R is a C₁-C₄ alkyl, aryl, phenyl, alkenyl, hydroxyl, a C₁-C₄ haloalkyl,halogen, or haloalkenyl; and R₁ is CH₃, CF₃, CH₂CH₃, or CF₂CF₃.
 33. Themethod of claim 32, wherein said SARM compound is represented by astructure of formula:

34-41. (canceled)
 42. A method of treating, preventing, suppressing orinhibiting metastasis in a subject suffering from breast cancer,comprising the step of administering to said subject a therapeuticallyeffective amount of a selective androgen receptor modulator (SARM)compound represented by a structure of formula I:

X is a bond, O, CH₂, NH, S, Se, PR, NO or NR; G is O or S; T is OH, OR,—NHCOCH₃, or NHCOR; R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl,CH₂F, CHF₂, CF₃, CF₂CF₃, aryl, phenyl, halogen, alkenyl or OH; R₁ isCH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃; R₂ is H, F, Cl, Br, I, CH₃,CF₃, OH, CN, NO₂, NHCOCH₃, NHCOCF₃, NHCOR, alkyl, arylalkyl, OR, NH₂,NHR, N(R)₂, SR; R₃ is H, F, Cl, Br, I, CN, NO₂, COR, COOH, CONHR, CF₃,Sn(R)₃, or R₃ together with the benzene ring to which it is attachedforms a fused ring system represented by the structure:

Z is NO₂, CN, COR, COOH, or CONHR; Y is CF₃, F, Br, Cl, I, CN, orSn(R)₃; Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃, NHCOR,NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃, NHSO₂R,OR, COR, OCOR, OSO₂R, SO₂R or SR; or Q together with the benzene ring towhich it is attached is a fused ring system represented by structure A,B or C:

n is an integer of 1-4; and m is an integer of 1-3.
 43. The method ofclaim 42, wherein said SARM compound is represented by a structure offormula XIII:

or formula XIV:


44. The method of claim 42, wherein said SARM compound is represented bya structure of formula II:

wherein X is a bond, O, CH₂, NH, Se, PR, or NR; G is O or S; T is OH,OR, —NHCOCH₃, or NHCOR; Z is NO₂, CN, COR, COOH or CONHR; Y is I, CF₃,Br, Cl, or Sn(R)₃; Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃,NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃,NHSO₂R, OR, COR, OCOR, OSO₂R, SO₂R or SR; or Q together with the benzenering to which it is attached is a fused ring system represented bystructure A, B or C:

R is a C₁-C₄ alkyl, aryl, phenyl, alkenyl, hydroxyl, a C₁-C₄ haloalkyl,halogen, or haloalkenyl; and R₁ is CH₃, CF₃, CH₂CH₃, or CF₂CF₃.
 45. Themethod of claim 44, wherein said SARM compound is represented by astructure of formula:

46-47. (canceled)
 48. The method of claim 42, wherein said breast canceris metastatic breast cancer; refractory breast cancer; AR-positivebreast cancer; AR-positive refractory breast cancer; AR-positivemetastatic breast cancer; triple negative breast cancer; advanced breastcancer; and/or breast cancer that has failed selective estrogen receptormodulator (tamoxifen, toremifene), aromatase inhibitor, trastuzumab(Herceptin, ado-trastuzumab emtansine), pertuzumab (Perjeta), lapatinib,exemestane (Aromasin), bevacizumab (Avastin), and/or fulvestranttreatments.
 49. A method of prolonging survival of a subject sufferingfrom breast cancer, or prolonging the progression-free survival of asubject suffering from breast cancer comprising the step ofadministering to said subject a selective androgen receptor modulator(SARM) compound represented by a structure of formula I:

X is a bond, O, CH₂, NH, S, Se, PR, NO or NR; G is O or S; T is OH, OR,—NHCOCH₃, or NHCOR; R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl,CH₂F, CHF₂, CF₃, CF₂CF₃, aryl, phenyl, halogen, alkenyl or OH; R₁ isCH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃; R₂ is H, F, Cl, Br, I, CH₃,CF₃, OH, CN, NO₂, NHCOCH₃, NHCOCF₃, NHCOR, alkyl, arylalkyl, OR, NH₂,NHR, N(R)₂, SR; R₃ is H, F, Cl, Br, I, CN, NO₂, COR, COOH, CONHR, CF₃,Sn(R)₃, or R₃ together with the benzene ring to which it is attachedforms a fused ring system represented by the structure:

Z is NO₂, CN, COR, COOH, or CONHR; Y is CF₃, F, Br, Cl, I, CN, orSn(R)₃; Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃, NHCOR,NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃, NHSO₂R,OR, COR, OCOR, OSO₂R, SO₂R or SR; or Q together with the benzene ring towhich it is attached is a fused ring system represented by structure A,B or C:

n is an integer of 1-4; and m is an integer of 1-3.
 50. The method ofclaim 49, wherein said SARM compound is represented by a structure offormula XIII:

or formula XIV:


51. The method of claim 49, wherein said SARM compound is represented bya structure of formula II:

wherein X is a bond, O, CH₂, NH, Se, PR, or NR; G is O or S; T is OH,OR, —NHCOCH₃, or NHCOR; Z is NO₂, CN, COR, COOH or CONHR; Y is I, CF₃,Br, Cl, or Sn(R)₃; Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃,NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃,NHSO₂R, OR, COR, OCOR, OSO₂R, SO₂R or SR; or Q together with the benzenering to which it is attached is a fused ring system represented bystructure A, B or C:

R is a C₁-C₄ alkyl, aryl, phenyl, alkenyl, hydroxyl, a C₁-C₄ haloalkyl,halogen, or haloalkenyl; and R₁ is CH₃, CF₃, CH₂CH₃, or CF₂CF₃.
 52. Themethod of claim 51, wherein said SARM compound is represented by astructure of formula:

53-54. (canceled)
 55. The method of claim 49, wherein said breast canceris metastatic breast cancer; refractory breast cancer; AR-positivebreast cancer; AR-positive refractory breast cancer; AR-positivemetastatic breast cancer; triple negative breast cancer; advanced breastcancer; and/or breast cancer that has failed selective estrogen receptormodulator SERM (tamoxifen, toremifene), aromatase inhibitor, trastuzumab(Herceptin, ado-trastuzumab emtansine), pertuzumab (Perjeta), lapatinib,exemestane (Aromasin), bevacizumab (Avastin), and/or fulvestranttreatments. 56.-62. (canceled)
 63. A method of treating a subjectsuffering from ER-positive breast cancer, comprising the step ofadministering to said subject a selective androgen receptor modulator(SARM) compound represented by a structure of formula I:

X is a bond, O, CH₂, NH, S, Se, PR, NO or NR; G is O or S; T is OH, OR,—NHCOCH₃, or NHCOR; R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl,CH₂F, CHF₂, CF₃, CF₂CF₃, aryl, phenyl, halogen, alkenyl or OH; R₁ isCH₃, CH₂F, CHF₂, CF₃, CH₂CH₃, or CF₂CF₃; R₂ is H, F, Cl, Br, I, CH₃,CF₃, OH, CN, NO₂, NHCOCH₃, NHCOCF₃, NHCOR, alkyl, arylalkyl, OR, NH₂,NHR, N(R)₂, SR; R₃ is H, F, Cl, Br, I, CN, NO₂, COR, COOH, CONHR, CF₃,Sn(R)₃, or R₃ together with the benzene ring to which it is attachedforms a fused ring system represented by the structure:

Z is NO₂, CN, COR, COOH, or CONHR; Y is CF₃, F, Br, Cl, I, CN, orSn(R)₃; Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃, NHCOR,NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃, NHSO₂R,OR, COR, OCOR, OSO₂R, SO₂R or SR; or Q together with the benzene ring towhich it is attached is a fused ring system represented by structure A,B or C:

n is an integer of 1-4; and m is an integer of 1-3.
 64. The method ofclaim 63, wherein said SARM compound is represented by a structure offormula XIII:

or formula XIV:


65. The method of claim 63, wherein said SARM compound is represented bya structure of formula II:

wherein X is a bond, O, CH₂, NH, Se, PR, or NR; G is O or S; T is OH,OR, —NHCOCH₃, or NHCOR; Z is NO₂, CN, COR, COOH or CONHR; Y is I, CF₃,Br, Cl, or Sn(R)₃; Q is CN, alkyl, halogen, N(R)₂, NHCOCH₃, NHCOCF₃,NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH₃, NHCSCF₃, NHCSRNHSO₂CH₃,NHSO₂R, OR, COR, OCOR, OSO₂R, SO₂R or SR; or Q together with the benzenering to which it is attached is a fused ring system represented bystructure A, B or C:

R is a C₁-C₄ alkyl, aryl, phenyl, alkenyl, hydroxyl, a C₁-C₄ haloalkyl,halogen, or haloalkenyl; and R₁ is CH₃, CF₃, CH₂CH₃, or CF₂CF₃.
 66. Themethod of claim 65, wherein said SARM compound is represented by astructure of formula:

67-68. (canceled)
 69. The method of claim 65, wherein said ER-positivebreast cancer is AR-positive.
 70. The method of claim 65, wherein saidER-positive breast cancer is AR-negative
 71. The method of claim 22,wherein said AR-positive breast cancer is ER-negative.
 72. The method ofclaim 22, wherein said AR-positive breast cancer is ER-negative,PR-negative and HER2 negative.
 73. The method of claim 22, wherein saidAR-positive breast cancer is ER-negative, PR-negative and HER2 positive.74. The method of claim 22, wherein said AR-positive breast cancer isER-negative, PR-positive and HER2 negative.
 75. The method of claim 22,wherein said AR-positive breast cancer is ER-positive, PR-negative andHER2 negative.
 76. The method of claim 22, wherein said AR-positivebreast cancer is ER-positive, PR-positive and HER2 negative.
 77. Themethod of claim 22, wherein said AR-positive breast cancer isER-positive, PR-negative and HER2 positive.
 78. The method of claim 22,wherein said AR-positive breast cancer is ER-negative, PR-positive andHER2 positive.
 79. The method of claim 1, comprising administering anisomer, a racemic mixture containing a SARM compound, a metabolite,pharmaceutically acceptable salt, pharmaceutical product, hydrate,N-oxide, or crystal of said selective androgen receptor modulator, orany combination thereof.
 80. The method of claim 79, wherein saidadministering comprises intravenously, intraarterially, orintramuscularly injecting to said subject said pharmaceutical product inliquid form; subcutaneously implanting in said subject a pelletcontaining said pharmaceutical product; orally administering to saidsubject said pharmaceutical product in a liquid or solid form; ortopically applying to the skin surface of said subject saidpharmaceutical product.
 81. The method of claim 80, wherein saidpharmaceutical product is a pellet, a tablet, a capsule, a solution, asuspension, an emulsion, an elixir, a gel, a cream, a suppository or aparenteral formulation.
 82. The method of claim 8, comprisingadministering an isomer, a racemic mixture containing a SARM compound, ametabolite, pharmaceutically acceptable salt, pharmaceutical product,hydrate, N-oxide, or crystal of said selective androgen receptormodulator, or any combination thereof.
 83. The method of claim 15,comprising administering an isomer, a racemic mixture containing a SARMcompound, a metabolite, pharmaceutically acceptable salt, pharmaceuticalproduct, hydrate, N-oxide, or crystal of said selective androgenreceptor modulator, or any combination thereof.
 84. The method of claim22, comprising administering an isomer, a racemic mixture containing aSARM compound, a metabolite, pharmaceutically acceptable salt,pharmaceutical product, hydrate, N-oxide, or crystal of said selectiveandrogen receptor modulator, or any combination thereof.
 85. The methodof claim 30, comprising administering an isomer, a racemic mixturecontaining a SARM compound, a metabolite, pharmaceutically acceptablesalt, pharmaceutical product, hydrate, N-oxide, or crystal of saidselective androgen receptor modulator, or any combination thereof. 86.The method of claim 42, comprising administering an isomer, a racemicmixture containing a SARM compound, a metabolite, pharmaceuticallyacceptable salt, pharmaceutical product, hydrate, N-oxide, or crystal ofsaid selective androgen receptor modulator, or any combination thereof.87. The method of claim 49, comprising administering an isomer, aracemic mixture containing a SARM compound, a metabolite,pharmaceutically acceptable salt, pharmaceutical product, hydrate,N-oxide, or crystal of said selective androgen receptor modulator, orany combination thereof.
 88. The method of claim 63, comprisingadministering an isomer, a racemic mixture containing a SARM compound, ametabolite, pharmaceutically acceptable salt, pharmaceutical product,hydrate, N-oxide, or crystal of said selective androgen receptormodulator, or any combination thereof